67714-30-1

Basic information

• Product Name: S-benzoyl-3-mercaptopropanoyl chloride
• Synonyms: S-benzoyl-3-mercaptopropanoyl chloride
• CAS NO: 67714-30-1
• Molecular Weight: 228.699
• Mol File: 67714-30-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: S-benzoyl-3-mercaptopropanoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: S-benzoyl-3-mercaptopropanoyl chloride(67714-30-1)
• EPA Substance Registry System: S-benzoyl-3-mercaptopropanoyl chloride(67714-30-1)

Safety Data

• Hazardous Substances Data: 67714-30-1(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 79-37-8 oxalyl dichloride 
• 6183-02-4 (+/-)-S-benzoyl-2-mercaptopropanoic acid 

Downstream Products

• 82562-40-1 (R)-3-(3-Benzoylsulfanyl-propionyl)-2-phenyl-thiazolidine-4-carboxylic acid 
• 82562-40-1 (2R,4R)-3-(3-Benzoylsulfanyl-propionyl)-2-phenyl-thiazolidine-4-carboxylic acid 
• 82562-41-2 (2S,4R)-3-(3-Benzoylsulfanyl-propionyl)-2-phenyl-thiazolidine-4-carboxylic acid 
• 105755-07-5 2-(3-Benzoylsulfanyl-propionylamino)-4-methylsulfanyl-butyric acid isopropyl ester 
• 72636-15-8 N,O-bis(S-benzoyl-3-mercaptopropanoyl)-L-tyrosine 
• 67362-18-9 (4R)-3-(S-benzoyl-3-mercaptopropanoyl)-4-thiazolidinecarboxylic acid 
• 91273-44-8 trans-N-(3-benzoylthio-1-oxopropyl)-N-(4-phenylcyclohexyl)glycine-1,1-dimethylethyl ester 
• 101895-58-3 N-(4-benzoylmercapto-2-oxo-butyl)-phthalimide 
• 162968-34-5 1,3-bis<<<6-(3-(benzoylmercapto)propionylamino)pyrid-2-yl>amino>carbonyl>-5-(heptyloxy)benzene 
• 78818-49-2 N²-(S-benzoyl-3-mercaptopropanoyl)-D-tryptophan 
• 82625-83-0 (4R)-3-(S-benzoyl-3-mercaptopropanoyl)-2,2-dimethyl-4-thiazolidinecarboxylic acid 
• 72678-42-3 (R)-3-(3-Benzoylsulfanyl-propionyl)-2-(2-hydroxy-3-methoxy-phenyl)-thiazolidine-4-carboxylic acid 
• 87459-76-5 N-(3-benzoilmercaptopropionil)-DL-metionina 
• 75664-12-9 (+/-)-1-<3-(benzoylthio)propionyl>-5-(2-hydroxyphenyl)-2-pyrrolidinecarboxylic acid 

Relevant articles and documents

SYNTHETIC HYDROGEN BONDING RECEPTORS AS MODELS OF TRANSACYLASE ENZYMES

A family of synthetic receptors has been prepared containing a barbiturate binding site and an appended thiol nucleophile.These are shown to cause large accelerations in the thiolysis reactions of barbiturate active ester derivatives.The size of the acceleration is shown to depend critically on the length and flexibility of the spacer that links the thiol to the receptor.