65236-05-7

Basic information

• Product Name: Carbamothioic acid, cyclohexyl-, S-(4-methoxyphenyl) ester
• CAS NO: 65236-05-7
• Molecular Formula: C14H19NO2S
• Molecular Weight: 265.376
• Mol File: 65236-05-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Carbamothioic acid, cyclohexyl-, S-(4-methoxyphenyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamothioic acid, cyclohexyl-, S-(4-methoxyphenyl) ester(65236-05-7)
• EPA Substance Registry System: Carbamothioic acid, cyclohexyl-, S-(4-methoxyphenyl) ester(65236-05-7)

Safety Data

• Hazardous Substances Data: 65236-05-7(Hazardous Substances Data)

Upstream product

• 696-63-9 4-Methoxybenzenethiol 
• 3173-53-3 Cyclohexyl isocyanate 
• 931-53-3 Cyclohexyl isocyanide 
• 98-68-0 4-methoxy-phenyl-sulphonyl chloride 
• 696-62-8 para-iodoanisole 

Relevant articles and documents

Synthesis of carbamothioate derivatives via a copper catalyzed thiocarboxamidation of aryl iodides

Abstract: A catalytic route to carbamothioate derivatives through a reaction involving isocyanides, elemental sulfur, and aryl iodides has been developed. The reaction scope has been examined using a range of isocyanides and aryl iodides. The reactions involve two consecutive C–S bond formations. Control experiment revealed that the reaction proceeds through an iminium species. Graphic abstract: [Figure not available: see fulltext.].

Molecular iodine-mediated synthesis of thiocarbamates from thiols, isocyanides and water under metal-free conditions

A simple and practical molecular iodine-mediated method for the efficient construction of thiocarbamates from isocyanides, thiols and water under metal-free and mild conditions has been developed. A variety of thiocarbamates were easily synthesized through this methodology, which has the advantages of simple operation, eco-friendly conditions, good functional group tolerance, and readily accessible raw materials.

Method of controlling pea aphids

Novel S-aryl N-cycloalkylthiolcarbamates, such as S-4-methoxy-phenyl N-cyclohexylthiolcarbamate, which are useful for controlling pea aphids, and the method of controlling pea aphids with the compounds are disclosed.