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Carbonochloridimidothioic acid, [(4-methylphenyl)sulfonyl]-, methyl ester is a complex organic compound with the chemical formula C9H10ClNOS2. It is a derivative of carbonochloridimidothioic acid, featuring a methyl group attached to the sulfur atom and a 4-methylphenylsulfonyl group connected to the nitrogen atom. Carbonochloridimidothioic acid, [(4-methylphenyl)sulfonyl]-, methyl ester is characterized by its unique structure, which includes a carbonyl group, a chloroimidothio group, and a methyl ester group. It is synthesized through a series of chemical reactions and is used in various applications, such as in the synthesis of pharmaceuticals and agrochemicals, due to its reactivity and functional group diversity. The compound's properties, such as its solubility and stability, are influenced by the presence of these functional groups, making it a versatile building block in organic chemistry.

2973-83-3

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2973-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2973-83-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2973-83:
(6*2)+(5*9)+(4*7)+(3*3)+(2*8)+(1*3)=113
113 % 10 = 3
So 2973-83-3 is a valid CAS Registry Number.

2973-83-3Relevant academic research and scientific papers

Synthesis of Cyclic Guanidines Bearing N-Arylsulfonyl and N-Cyano Protecting Groups via Pd-Catalyzed Alkene Carboamination Reactions

Peterson, Luke J.,Luo, Jingyi,Wolfe, John P.

, p. 2817 - 2820 (2017)

Palladium-catalyzed carboamination reactions of N-allylguanidines bearing cleavable N-cyano or N-arylsulfonyl protecting groups are described. The reactions afford cyclic guanidine products in good yield, and transformations of substrates bearing internal alkenes proceed with high diastereoselectivity. Deuterium labeling studies indicate these transformations proceed via anti-aminopalladation pathways.

Intramolecular Formation of Zwitterionic Intermediates in 1,3-Diaza-Claisen Rearrangements

Walker, Joel D.,Watson, Rebecca,Flemer, Stevenson,Yang, Yanbo,Madalengoitia, José S.

supporting information, p. 4010 - 4013 (2017/08/14)

Isothioureas tethered to bridged-bicyclic tertiary allylic amines can be converted to carbodiimides through reaction with Hg(II) salts. Intramolecular cyclization of the tethered tertiary allylic amines to the carbodiimides afford zwitterionic intermediat

Synthesis of Cyclic Guanidines via Silver-Catalyzed Intramolecular Alkene Hydroamination Reactions of N-Allylguanidines

Garlets, Zachary J.,Silvi, Mattia,Wolfe, John P.

supporting information, p. 2331 - 2334 (2016/06/09)

The silver-catalyzed hydroamination of tosyl-protected N-allylguanidines is described. These reactions provide substituted cyclic guanidines in high yields. The reactions are amenable to the construction of quaternary stereocenters as well as both monocyc

Strukturanalytische Untersuchungen an Folgeprodukten aus Sulfonamiden VI - Kinetische Untersuchungen zur Reaktion von N-Arylsulfonyl-iminothiokohlensaeuremethylesterchloriden mit aliphatischen Aminen

Hans, M.,Imrich, J.,Barnikol, F.,Reinke, H.,Suchar, G.,et al.

, p. 1089 - 1097 (2007/10/02)

The reaction of a number of N-arylsulfonyl-iminothiocarbonic acid methylesterchloride compounds 1 with nucleophiles is studied by means of stopped-flow analysis.To clarify the reaction mechanism the influence of concentration, solvents and substituents on

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