Tag: M.W=100-150

COA of Formula: C8H10O2. Authors Esteruelas, MA; Martinez, A; Olivan, M; Onate, E in AMER CHEMICAL SOC published article about in [Esteruelas, Miguel A.; Martinez, Antonio; Olivan, Montserrat; Onate, Enrique] Univ Zaragoza, Dept Quim Inorgan, Inst Sintesis Quim & Catalisis Homogenea ISQCH, Ctr Innovac Quim Avanzada ORFEO CINQA,CSIC, E-50009 Zaragoza, Spain in 2020, Cited 98. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0

The saturated trihydride IrH3{kappa(3)-P,O,P-[xant((PPr2)-Pr-i)(2)]) (1; xant((PPr2)-Pr-i)(2) = 9,9-dimethyl-4,5-bis(diisopropylphosphino)xanthene) coordinates the Si-H bond of triethylsilane, 1,1,1,3,5,5,5-heptamethyltrisiloxane, and triphenylsilane to give the sigma-complexes IrH3 (eta(2)-H-SiR3){kappa(2)-cis-P,P-[xant((PPr2)-Pr-i)(2)]}, which evolve to the dihydride-silyl derivatives IrH2(SiR3){kappa 3- P,O,P [xant((PPr2)-Pr-i)(2)]} (SiR3 = SiEt3 (2), SiMe(OSiMe3)(2) (3), SiPh3 (4)) by means of the oxidative addition of the coordinated bond and the subsequent reductive elimination of H-2. Complexes 2-4 activate a C-H bond of symmetrically and asymmetrically substituted arenes to form silylated arenes and to regenerate 1. This sequence of reactions defines a cycle for the catalytic direct C-H silylation of arenes. Stoichiometric isotopic experiments and the kinetic analysis of the transformations demonstrate that the C-H bond rupture is the rate-determining step of the catalysis. As a consequence, the selectivity of the silylation of substituted arenes is generally governed by ligand-substrate steric interactions.

About 1,3-Dimethoxybenzene, If you have any questions, you can contact Esteruelas, MA; Martinez, A; Olivan, M; Onate, E or concate me.. COA of Formula: C8H10O2

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

In 2019 CHEMSUSCHEM published article about PROTON ACCEPTOR GROUPS; X-RAY-DIFFRACTION; HYDROPHOBIC AMPLIFICATION; ORGANIC-REACTIONS; MICHAEL ADDITION; ALKYL; CATALYST; BENZENE; DIARYLMETHANES; ACCELERATION in [La Manna, Pellegrino; Soriente, Annunziata; De Rosa, Margherita; Buonerba, Antonio; Talotta, Carmen; Gaeta, Carmine; Neri, Placido] Univ Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II, I-84084 Salerno, Italy in 2019, Cited 98. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0. Formula: C8H10O2

Metal-free Friedel-Crafts benzylation (FCB) of scarcely reactive arenes and heteroarenes was performed under on-water conditions by an environmentally sustainable procedure. The catalytic strategy exploits the hydrophobicity of the resorcinarene macrocycle 1 a. The proposed mechanism is based on the activation of benzyl chloride by H-bonding interactions with catalyst 1 a. In fact, under on-water conditions the hydrophobic amplification of the strength of the H-bonding interactions between the OH groups of the resorcinarene catalyst and the chlorine atom of benzyl chloride leads to polarization of the C-Cl bond, which consequently promotes electrophilic attack of the pi nucleophile. Thus, many arenes and heteroarenes were efficiently benzylated under mild on-water conditions by using resorcinarene 1 a as catalyst. The FCB of benzene is industrially relevant for the synthesis of diphenylmethane, and hence the on-water procedure was extended to the gram-scale synthesis of diphenylmethane, starting from benzene and benzyl chloride in the presence of resorcinarene catalyst 1 a.

Formula: C8H10O2. About 1,3-Dimethoxybenzene, If you have any questions, you can contact La Manna, P; Soriente, A; De Rosa, M; Buonerba, A; Talotta, C; Gaeta, C; Neri, P or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Wang, FF; Li, XY; Li, ZY; Zhou, SL; Zhang, W in [Wang, Feifan; Li, Xiaoyue; Li, Zhongyu; Zhou, Shuangliu; Zhang, Wu] Anhui Normal Univ, Coll Chem & Mat Sci, Wuhu 241000, Peoples R China; [Zhou, Shuangliu; Zhang, Wu] Anhui Normal Univ, Key Lab Funct Mol Solids, Minist Educ, Wuhu 241000, Peoples R China published Copper Salts/TBAB-Catalyzed Chemo- and Regioselective beta-C(sp(3))-H Acyloxylation of Aliphatic Amides in 2019, Cited 80. COA of Formula: C8H8O2. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7.

An efficient Cu(II)-catalyzed and tetrabutylammonium bromide (TBAB)-promoted strategy for highly regioselective and chemoselective C(sp(3))-H acyloxylation of aliphatic amides is described. Acyloxylation occurs selectively at the beta position with a broad substrate scope of carboxylic acids and aliphatic amides and good functional group compatibility. Notably, the competing reaction of intramolecular dehydrogenative amidation and intermolecular acyloxylation could be efficiently controlled by the amount of copper salt and the addition of TBAB. The intramolecular dehydrogenative amidation product was obtained in high yield when the amount of copper salts was increased. However, when TBAB was used as an additive, a preference for acyloxylation over intramolecular amidation was observed and the acyloxylated products were obtained in good yield. Preliminary studies were carried out to gain insights into the mechanism.

COA of Formula: C8H8O2. About 3-Methylbenzoic acid, If you have any questions, you can contact Wang, FF; Li, XY; Li, ZY; Zhou, SL; Zhang, W or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Ray, P; Hughes, T; Smith, C; Hibbert, M; Saito, K; Simon, GP in [Ray, Parijat; Simon, George P.] Monash Univ, Dept Mat Sci & Engn, Clayton, Vic 3800, Australia; [Hughes, Timothy; Saito, Kei] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia; [Smith, Craig] PPG Ind Inc, Springdale, PA 15144 USA; [Hibbert, Mena] PPG Ind Australia Pty Ltd, Clayton, Vic 3168, Australia published Development of bio-acrylic polymers from Cyrene (TM): transforming a green solvent to a green polymer in 2019, Cited 26. Application In Synthesis of 1,3-Dimethoxybenzene. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0.

In this work, Cyrene (TM), a bio-based green solvent, has been transformed into its methacrylic derivative (m-Cyrene) for the first time. Polymerization of the newly-synthesized monomer was studied using different polymerization techniques such as bulk, solution and emulsion polymerization. Compared to solution polymerization, emulsion polymerization was found to produce higher yields and molecular weights. Cyrene (TM), along with other green solvents, was used as a polymerization solvent and was found to be the most effective (as a solvent) with the highest yield and molecular weight. The new Cyrene (TM) monomer was found to undergo rapid polymerization compared to isobornyl methacrylate (IBMA), another bio-derived monomer with a close structural similarity, and the highest polymerization rate was obtained in Cyrene (TM) as the polymerization solvent media. A reactivity ratio calculation also showed m-Cyrene to be more reactive than IBMA. The homopolymer derived from emulsion polymerization showed high glass transition temperature (192 degrees C) and thermal stability (up to ca. 266 degrees C). Cytotoxicity testing confirmed the non-toxic nature of the bio-derived monomer, making it a green bio-derived methacrylic monomer for synthesizing polymers, where high thermal stability and mechanical properties are required.

Application In Synthesis of 1,3-Dimethoxybenzene. About 1,3-Dimethoxybenzene, If you have any questions, you can contact Ray, P; Hughes, T; Smith, C; Hibbert, M; Saito, K; Simon, GP or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

An article Quantifications and Applications of Relative Fisher Information in Density Functional Theory WOS:000648873600028 published article about SUBSTITUTED FULVENE DERIVATIVES; MOLECULAR ACIDITY; ELECTRONIC-PROPERTIES; ROTATION BARRIERS; REACTIVITY; HIRSHFELD; ELECTROPHILICITY; AROMATICITY; QUANTITIES; ENERGY in [Wang, Bin; Rong, Chunying] Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med Res, Minist Educ China, Changsha 410081, Hunan, Peoples R China; [Lu, Tian] Beijing Kein Res Ctr Nat Sci, Beijing 100022, Peoples R China; [Zhao, Dongbo] Yunnan Univ, Inst Biomed Res, Kunming 650500, Yunnan, Peoples R China; [Liu, Shubin] Univ N Carolina, Res Comp Ctr, Chapel Hill, NC 27599 USA in 2021, Cited 79. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0. Safety of 1,3-Dimethoxybenzene

Though density functional theory is widely accepted as one of the most successful developments in theoretical chemistry in the past few decades, the knowledge of how to apply this new electronic structure theory, to help us better understand chemical processes and transformations, is still an unaccomplished task. The information-theoretic approach is emerging as a viable option for that purpose in the recent literature, providing new insights about steric effect, cooperativity, electrophilicity, nucleophilicity, stereoselectivity, homochirality, etc. In this work, based on the result from a recent paper by one of us [J. Chem. Phys, 2019, 151, 141103], we present two quantifications of the relative Fisher information and discuss their physiochemical properties and possible applications. To that end, their analytical properties have been elucidated. They have also been applied to six categories of systems to illustrate their applicability. A better descriptor to quantify the single bond rotation barrier has been obtained. The relative Fisher information can also simultaneously determine electrophilicity and nucleophilicity, and effectively describe helical structures with different homochiral and heterochiral propensities. As integral parts of the information-theoretic approach, these newly introduced quantities will provide us with more analytical tools toward the long-term goal of crafting a chemical reactivity theory in the density-based language.

Safety of 1,3-Dimethoxybenzene. About 1,3-Dimethoxybenzene, If you have any questions, you can contact Wang, B; Zhao, DB; Lu, T; Liu, SB; Rong, CY or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Authors Goncharova, IK; Silaeva, KP; Arzumanyan, AV; Anisimov, AA; Milenin, SA; Novikov, RA; Solyev, PN; Tkachev, YV; Volodin, AD; Korlyukov, AA; Muzafarov, AM in AMER CHEMICAL SOC published article about N-HYDROXYPHTHALIMIDE; COPOLYMERS; STRATEGIES; POLYDIMETHYLSILOXANE; CONSTRUCTION; MORPHOLOGY; CHEMISTRY; POLYMERS; SILANOLS; POLAR in [Goncharova, Irina K.; Silaeva, Kseniia P.; Arzumanyan, Ashot V.; Anisimov, Anton A.; Volodin, Alexander D.; Korlyukov, Alexander A.; Muzafarov, Aziz M.] Russian Acad Sci, Nesmeyanov Inst Organoelement Cpds, 28 Vavilova St, Moscow 119991, Russia; [Silaeva, Kseniia P.] Mendeleev Univ Chem Technol Russia, 9 Miusskaya Sq, Moscow 125047, Russia; [Milenin, Sergey A.; Muzafarov, Aziz M.] Russian Acad Sci, Enikolopov Inst Synthet Polymer Mat, 70 Profsoyuznaya St, Moscow 117393, Russia; [Novikov, Roman A.; Solyev, Pavel N.; Tkachev, Yaroslav V.] Russian Acad Sci, Engelhardt Inst Mol Biol, 32 Vavilova St, Moscow 119991, Russia; [Korlyukov, Alexander A.] Pirogov Russian Natl Res Med Univ, 1 Ostrovityanov St, Moscow 117997, Russia; [Novikov, Roman A.] Russian Acad Sci, Zelinsky Inst Organ Chem, 47 Leninsky Pr, Moscow 119991, Russia in 2019.0, Cited 75.0. Safety of 3-Methylbenzoic acid. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7

Synthesis of organosilicon products with a polar functional group within organic substituents is one of the most fundamentally and practically important challenges in today’s chemistry of silicones. In our study, we suggest a solution to this problem, viz., a high-efficiency preparative method based on aerobic Co-/N-hydroxysuccinimide (NHSI) catalyzed oxidation of p-tolylsiloxanes to p-carboxyphenylsiloxanes. This approach is based on green, commercially available, simple, and inexpensive reagents and employs mild reaction conditions: Co(OAc)(2)/NHSI catalytic system, O-2 as the oxidant, process temperature from 40 to 60 degrees C, atmospheric pressure. This reaction is general and allows for synthesizing both mono-and di-, tri-, and poly(p-carboxyphenyl)siloxanes with p-carboxyphenyl groups at 1,1-, 1,3-, 1,5-, and 1,1,1-positions. All the products were obtained and isolated in gram amounts (up to 5 g) and in high yields (80-96%) and characterized by NMR, ESI-HRMS, GPC, IR, and X-ray data: p-carboxyphenylsiloxanes in crystalline state form HOF-like structures. Furthermore, it was shown that the suggested method is applicable for the oxidation of organic alkylarene derivatives (Ar-CH3, Ar-CH2-R) to the corresponding acids and ketones (Ar-C(O)OH and Ar-C(O)-R), as well as hydride silanes ([Si]-H) to silanols ([Si]-OH). The possibility of synthesizing monomeric (methyl) and polymeric (siloxane-containing PET analogue, Sila-PET) esters based on 1,3-bis(p-carboxyphenyl)disiloxane was studied. These processes occur with retention of the organosiloxane frame and allow to obtain the corresponding products in 90 and 99% yields.

About 3-Methylbenzoic acid, If you have any questions, you can contact Goncharova, IK; Silaeva, KP; Arzumanyan, AV; Anisimov, AA; Milenin, SA; Novikov, RA; Solyev, PN; Tkachev, YV; Volodin, AD; Korlyukov, AA; Muzafarov, AM or concate me.. Safety of 3-Methylbenzoic acid

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Formula: C8H10O2. Lin, HS; Okawa, S; Ma, Y; Yotsumoto, S; Lee, C; Tan, S; Manzhos, S; Yoshizawa, M; Chiashi, S; Lee, HM; Tanaka, T; Kataura, H; Jeon, I; Matsuo, Y; Maruyama, S in [Jeon, Il] Pusan Natl Univ, Inst Plast Informat & Energy Mat, Grad Sch Chem Mat, Dept Chem Educ, Busan 46241, South Korea; [Lin, Hao-Sheng; Okawa, Shunhei; Yotsumoto, Satoshi; Chiashi, Shohei; Jeon, Il; Matsuo, Yutaka; Maruyama, Shigeo] Univ Tokyo, Dept Mech Engn, Tokyo 1138656, Japan; [Matsuo, Yutaka] Nagoya Univ, Inst Mat Innovat, Inst Innovat Future Soc, Nagoya, Aichi 4648603, Japan; [Tanaka, Takeshi; Kataura, Hiromichi; Maruyama, Shigeo] Natl Inst Adv Ind Sci & Technol, Nanomat Res Inst, Tsukuba, Ibaraki 3058565, Japan; [Ma, Yue] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China; [Lee, Changsoo; Lee, Hyuck Mo] Korea Adv Inst Sci & Technol KAIST, Dept Mat Sci & Engn, Daejeon 34141, South Korea; [Tan, Shaun] Univ Calif Los Angeles, Dept Mat Sci & Engn, Los Angeles, CA 90095 USA; [Manzhos, Sergei] Inst Natl Rech Sci, Ctr Energie Mat Telecommun, Varennes, PQ, Canada; [Yoshizawa, Michito] Tokyo Inst Technol, Inst Innovat Res, Lab Chem & Life Sci, Yokohama, Kanagawa 2268503, Japan published Polyaromatic Nanotweezers on Semiconducting Carbon Nanotubes for the Growth and Interfacing of Lead Halide Perovskite Crystal Grains in Solar Cells in 2020, Cited 55. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0.

Perovskite crystal grain size control, grain boundary passivation, and grain bridging are the keys to obtaining high efficiency in perovskite solar cells. A small amount of semi-conducting single-walled carbon nanotubes added to a perovskite active layer can achieve this. In particular, the surfactants attached to the semiconducting single-walled carbon nanotubes a crucial role. In this work, we synthesized a new surfactant, 4,6-di(anthracen-9-yl)-1,3-phenylene bis(dimethylcarbamate), which has a polyaromatic group on one end and a urea-analogue carbamate group on the other end. The polyaromatic anthracene end functions as a nanotweezer clenching the carbon nanotubes strongly via pi-pi interaction while the carbamate end interacts with Pb2+, functioning as a strong Lewis base. In addition, the new surfactant has conjugated double bonds with a suitable bandgap, resulting in enhanced charge mobility in the perovskite film. Overall, the new surfactant-clenched semiconducting carbon nanotubes showcase superior effectiveness as passivators and charge bridges in perovskite solar cells as compared to the conventional deoxycholate surfactant-wrapped semiconducting single-walled carbon nanotubes. The new surfactant-attached semiconducting carbon nanotube-added NH3CH3PbI3-based perovskite solar cells exhibited a power conversion efficiency of 20.7%, which is higher than that of the reference devices with no additives (18.4%) and the previously reported semiconducting single-walled carbon nanotube-added devices (19.7% in this work and 19.5% in the literature).

Formula: C8H10O2. About 1,3-Dimethoxybenzene, If you have any questions, you can contact Lin, HS; Okawa, S; Ma, Y; Yotsumoto, S; Lee, C; Tan, S; Manzhos, S; Yoshizawa, M; Chiashi, S; Lee, HM; Tanaka, T; Kataura, H; Jeon, I; Matsuo, Y; Maruyama, S or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Recommanded Product: 1,3-Dimethoxybenzene. In 2020 ACS OMEGA published article about QUINONES in [Yu, Huangchao; Fought, Ellie L.; Windus, Theresa L.; Kraus, George A.] Iowa State Univ, Dept Chem, Ames, IA 50011 USA in 2020, Cited 15. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0.

A variety of nucleophiles react efficiently with in situ generated nitroquinones. The reaction with substituted resorcinols led to the direct synthesis of the phenanthroviridinone and lagumycin skeleton via a highly regioselective Diels-Alder reaction.

About 1,3-Dimethoxybenzene, If you have any questions, you can contact Yu, HC; Fought, EL; Windus, TL; Kraus, GA or concate me.. Recommanded Product: 1,3-Dimethoxybenzene

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

In 2019.0 J AM CHEM SOC published article about N-HYDROXYPHTHALIMIDE; COPOLYMERS; STRATEGIES; POLYDIMETHYLSILOXANE; CONSTRUCTION; MORPHOLOGY; CHEMISTRY; POLYMERS; SILANOLS; POLAR in [Goncharova, Irina K.; Silaeva, Kseniia P.; Arzumanyan, Ashot V.; Anisimov, Anton A.; Volodin, Alexander D.; Korlyukov, Alexander A.; Muzafarov, Aziz M.] Russian Acad Sci, Nesmeyanov Inst Organoelement Cpds, 28 Vavilova St, Moscow 119991, Russia; [Silaeva, Kseniia P.] Mendeleev Univ Chem Technol Russia, 9 Miusskaya Sq, Moscow 125047, Russia; [Milenin, Sergey A.; Muzafarov, Aziz M.] Russian Acad Sci, Enikolopov Inst Synthet Polymer Mat, 70 Profsoyuznaya St, Moscow 117393, Russia; [Novikov, Roman A.; Solyev, Pavel N.; Tkachev, Yaroslav V.] Russian Acad Sci, Engelhardt Inst Mol Biol, 32 Vavilova St, Moscow 119991, Russia; [Korlyukov, Alexander A.] Pirogov Russian Natl Res Med Univ, 1 Ostrovityanov St, Moscow 117997, Russia; [Novikov, Roman A.] Russian Acad Sci, Zelinsky Inst Organ Chem, 47 Leninsky Pr, Moscow 119991, Russia in 2019.0, Cited 75.0. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7. Name: 3-Methylbenzoic acid

Synthesis of organosilicon products with a polar functional group within organic substituents is one of the most fundamentally and practically important challenges in today’s chemistry of silicones. In our study, we suggest a solution to this problem, viz., a high-efficiency preparative method based on aerobic Co-/N-hydroxysuccinimide (NHSI) catalyzed oxidation of p-tolylsiloxanes to p-carboxyphenylsiloxanes. This approach is based on green, commercially available, simple, and inexpensive reagents and employs mild reaction conditions: Co(OAc)(2)/NHSI catalytic system, O-2 as the oxidant, process temperature from 40 to 60 degrees C, atmospheric pressure. This reaction is general and allows for synthesizing both mono-and di-, tri-, and poly(p-carboxyphenyl)siloxanes with p-carboxyphenyl groups at 1,1-, 1,3-, 1,5-, and 1,1,1-positions. All the products were obtained and isolated in gram amounts (up to 5 g) and in high yields (80-96%) and characterized by NMR, ESI-HRMS, GPC, IR, and X-ray data: p-carboxyphenylsiloxanes in crystalline state form HOF-like structures. Furthermore, it was shown that the suggested method is applicable for the oxidation of organic alkylarene derivatives (Ar-CH3, Ar-CH2-R) to the corresponding acids and ketones (Ar-C(O)OH and Ar-C(O)-R), as well as hydride silanes ([Si]-H) to silanols ([Si]-OH). The possibility of synthesizing monomeric (methyl) and polymeric (siloxane-containing PET analogue, Sila-PET) esters based on 1,3-bis(p-carboxyphenyl)disiloxane was studied. These processes occur with retention of the organosiloxane frame and allow to obtain the corresponding products in 90 and 99% yields.

About 3-Methylbenzoic acid, If you have any questions, you can contact Goncharova, IK; Silaeva, KP; Arzumanyan, AV; Anisimov, AA; Milenin, SA; Novikov, RA; Solyev, PN; Tkachev, YV; Volodin, AD; Korlyukov, AA; Muzafarov, AM or concate me.. Name: 3-Methylbenzoic acid

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

I found the field of Chemistry very interesting. Saw the article Synthesis of Bidentate Nitrogen Ligands by Rh-Catalyzed C-H Annulation and Their Application to Pd-Catalyzed Aerobic C-H Alkenylation published in 2021. HPLC of Formula: C8H10O2, Reprint Addresses Joo, JM (corresponding author), Pusan Natl Univ, Dept Chem & Chem, Inst Funct Mat, Busan 46241, South Korea.. The CAS is 151-10-0. Through research, I have a further understanding and discovery of 1,3-Dimethoxybenzene

A new class of bidentate ligands was prepared by a modular approach involving Rh-catalyzed C-H annulation reactions. The resulting conformationally constrained ligands enabled the Pd-catalyzed C-H alkenylation at electron-rich and sterically less hindered positions of electron-rich arenes while promoting the facile oxidation of Pd(0) intermediates by oxygen. This newly introduced ligand class is complementary to the ligands developed for Pd-catalyzed oxidative reactions and may find broad application in transition-metal-catalyzed reactions.

HPLC of Formula: C8H10O2. About 1,3-Dimethoxybenzene, If you have any questions, you can contact Kim, HT; Kang, E; Kim, M; Joo, JM or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com