2527-62-0

Basic information

• Product Name: Benzamide, 2,2'-dithiobis[N-(phenylmethyl)-
• CAS NO: 2527-62-0
• Molecular Formula: C28H24N2O2S2
• Molecular Weight: 484.643
• Mol File: 2527-62-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzamide, 2,2'-dithiobis[N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 2,2'-dithiobis[N-(phenylmethyl)-(2527-62-0)
• EPA Substance Registry System: Benzamide, 2,2'-dithiobis[N-(phenylmethyl)-(2527-62-0)

Safety Data

• Hazardous Substances Data: 2527-62-0(Hazardous Substances Data)

Upstream product

• 82082-50-6 N-benzyl-2-bromobenzamide 
• 147-93-3 Thiosalicylic acid 
• 119-80-2 2,2'-dithiobenzoic acid 
• 19602-82-5 2,2'-dithiodibenzoic acid dichloride 
• 100-46-9 benzylamine 
• 77586-83-5 2-trichloromethyl-3,1-benzoxathian-4-one 

Downstream Products

• 3260-92-2 2-acetyl-3-hydroxybenzo[b]thiophene 
• 24434-82-0 benzo[b]thiophen-3-yl acetate 
• 20054-55-1 3-benzyl-benzo[e][1,3]thiazine-2,4-dithione 
• 20054-65-3 3-benzyl-2-thio-2,3-dihydro-4H-benzothiazine-4-one 
• 10353-44-3 3-benzylbenzothiazine-2,4-dione 
• 2514-36-5 2-benzylbenzo[d]isothiazol-3(2H)-one 
• 15871-31-5 2-benzyl-2,3-dihydro-1,2-benzisothiazol-3-thion 
• 77586-93-7 N-(3H-1,2-benzodithiol-3-yliden)benzylamin 
• 13156-90-6 N-benzyl-2-mercaptobenzamide 
• 102478-82-0 N-benzyl-2-(benzylthio)benzamide 
• 3416-59-9 N-benzylsaccharin 

Relevant articles and documents

Preparation of benzisothiazolones from 2-bromobenzamides and sulfur under copper catalysis conditions

A convenient two-stage method has been developed for preparing benz[d]isothiazol-3(2H)-ones from 2-bromobenzamides and sulfur in a one-pot process under copper catalysis conditions. The method is suitable for the synthesis of N-aryl-, benzyl-, and alkyl-substituted benzisothiazolones. The yields of the benzisothiazolones depend on the nature of the starting amide and can reach 91%.

Cu and Ag catalyzed oxidative arylthiation of terminal acetylenes

A mild Cu or Ag catalyzed oxidative arylthiation of terminal acetylenes is introduced. The process, featuring metal catalyzed C-H bond activation as a key step, leads to the formation of highly substituted mercaptoacetylenes under unprecedented neutral conditions.

Antithrombotic agent

Certain 2,2'-dithiobis-N-substituted or unsubstituted benzamides or derivatives thereof are useful as antithrombotic agents because of their ability to suppress aggregation of blood platelets.