73721-89-8

Basic information

• Product Name: Benzamide, N-(2-mercaptoethyl)-
• CAS NO: 73721-89-8
• Molecular Formula: C9H11NOS
• Molecular Weight: 181.258
• Mol File: 73721-89-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzamide, N-(2-mercaptoethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(2-mercaptoethyl)-(73721-89-8)
• EPA Substance Registry System: Benzamide, N-(2-mercaptoethyl)-(73721-89-8)

Safety Data

• Hazardous Substances Data: 73721-89-8(Hazardous Substances Data)

Upstream product

• 151-56-4 ethyleneimine 
• 98-91-9 thiobenzoic acid 
• 5205-42-5 N,N'-(2,2'-disulfanediylbis(ethane-2,1-diyl))dibenzamide 
• 23405-15-4 benzoic acid N-hydroxysuccinimide ester 
• 729553-08-6 C₉H₁₁NO₄S₂ 
• 156-57-0 2-mercaptoethylamine hydrochloride 
• 98-88-4 benzoyl chloride 
• 60-23-1 Cysteamine 
• 99071-70-2 N-(2-thiocyanato-ethyl)-benzamide 
• 27110-61-8 N-(2-Bromo-ethyl)-benzamide 
• 65-85-0 benzoic acid 
• 243990-68-3 1-(2,5-Dichlorophenyl)-2,2-bis(methylsulfanyl)vinyl benzoate 
• 17612-90-7 S-benzoylcysteamine hydrochloride 

Downstream Products

• 92555-37-8 N-[2-(2,4-dinitro-phenylsulfanyl)-ethyl]-benzamide 
• 2722-34-1 2-phenylthiazoline 
• 5205-42-5 N,N'-(2,2'-disulfanediylbis(ethane-2,1-diyl))dibenzamide 
• 1137241-53-2 N-[2-(triphenylmethylsulfanyl)ethyl]benzamide 
• 55065-04-8 S-2-(N-benzoylamino)ethyl benzothioathe 
• 99855-18-2 1-acetylsulfanyl-2-benzoylamino-ethane 

Relevant articles and documents

Ammonia-borane as a Catalyst for the Direct Amidation of Carboxylic Acids

Ammonia-borane serves as an efficient substoichiometric (10%) precatalyst for the direct amidation of both aromatic and aliphatic carboxylic acids. In situ generation of amine-boranes precedes the amidation and, unlike the amidation with stoichiometric amine-boranes, this process is facile with 1 equiv of the acid. This methodology has high functional group tolerance and chromatography-free purification but is not amenable for esterification. The latter feature has been exploited to prepare hydroxyl- and thiol-containing amides.

Reduction with tris(2-carboxyethyl)phosphine (TCEP) enables the use of an S-sulphonate protecting group for thiol-mediated bioconjugation

Herein, we demonstrate the effectiveness of the water-friendly S-sulphonate group as an alternative to traditional thiol protecting groups for subsequent deprotection-bioconjugation reactions, under conditions that are compatible with the use of biochemic

CORROSION PROTECTION COATINGS

The present invention relates to new coating materials for corrosion control.