56741-04-9

Basic information

• Product Name: Carbamothioic acid, (1,1-dimethylethyl)-, S-phenyl ester
• CAS NO: 56741-04-9
• Molecular Formula: C11H15NOS
• Molecular Weight: 209.312
• Mol File: 56741-04-9.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Carbamothioic acid, (1,1-dimethylethyl)-, S-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamothioic acid, (1,1-dimethylethyl)-, S-phenyl ester(56741-04-9)
• EPA Substance Registry System: Carbamothioic acid, (1,1-dimethylethyl)-, S-phenyl ester(56741-04-9)

Safety Data

• Hazardous Substances Data: 56741-04-9(Hazardous Substances Data)

Upstream product

• 5285-87-0 phenyl thiocyanate 
• 115-11-7 isobutene 
• 201230-82-2 carbon monoxide 
• 75-64-9 tert-butylamine 
• 882-33-7 diphenyldisulfane 
• 1212-08-4 S-Phenyl benzenethiosulfonate 
• 2425-74-3 t-butylformamide 
• 591-50-4 iodobenzene 
• 119072-55-8 tert-butylisonitrile 
• 80-17-1 benzenesufonyl hydrazide 
• 108-98-5 thiophenol 
• 1146-42-5 p-methoxyphenylsulfonothioic phenyl ester 
• 98-09-9 benzenesulfonyl chloride 
• 873-55-2 sodium benzenesulfonate 

Downstream Products

• 882-33-7 diphenyldisulfane 
• 686-96-4 N-tert-butyltrimethylacetamide 
• 1579273-93-0 N-(tert-butyl)phenanthrene-9-carboxamide 
• 5894-65-5 N-t-butylbenzamide 
• 63064-23-3 N-(tert-butyl)-2,4,6-trimethylbenzamide 

Relevant articles and documents

Visible-light-promoted synthesis of secondary and tertiary thiocarbamates from thiosulfonates andN-substituted formamides

A general visible-light-promoted metal-free synthesis of secondary and tertiary thiocarbamates starting from thiosulfonates andN-substituted formamides is developed. By employing rhodamine B as a photocatalyst andtert-butyl hydroperoxide (TBHP) as an oxidant, a wide scope of thiocarbamates can be obtained through direct thiolation of acyl C-H bonds under irradiation of blue light at room temperature for 12 h.

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.].

Iodine-Catalyzed Odorless Synthesis of S-Thiocarbamates with Sulfonyl Chlorides as a Sulfur Source

A general and efficient protocol for the direct preparation of various S-thiocarbamates with readily available and inexpensive sulfonyl chlorides as an odorless sulfur source was developed. The employment of easily available reactants, excellent functiona