66552-53-2

Basic information

• Product Name: 2-Benzothiazolesulfenamide,N-propyl-(9CI)
• Synonyms: 2-Benzothiazolesulfenamide,N-propyl-(9CI)
• CAS NO: 66552-53-2
• Molecular Formula: C₁₀H₁₂N₂S₂
• Molecular Weight: 224.34568
• Product Categories: BENZOTHIAZOLE
• Mol File: 66552-53-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Benzothiazolesulfenamide,N-propyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Benzothiazolesulfenamide,N-propyl-(9CI)(66552-53-2)
• EPA Substance Registry System: 2-Benzothiazolesulfenamide,N-propyl-(9CI)(66552-53-2)

Safety Data

• Hazardous Substances Data: 66552-53-2(Hazardous Substances Data)

Upstream product

• 107-10-8 propylamine 
• 149-30-4 2-thioxo-3H-1,3-benzothiazole 
• 149-30-4 2-Mercaptobenzothiazole 
• 120-78-5 di(benzothiazol-2-yl)disulfide 

Downstream Products

• 74124-45-1 Phosphorsaeurediisopropylester-propylamid 
• 75291-14-4 Thiophosphoric acid S-benzothiazol-2-yl ester O,O'-diisopropyl ester 
• 149-30-4 2-Mercaptobenzothiazole 
• 2672-32-4 propyl-amidophosphoric acid diethyl ester 
• 615-22-5 2-methylmercaptobenzothiazole 
• 20465-00-3 N-Propyl-O,O-dimethyl-phosphorsaeureamid 

Relevant articles and documents

Scalable electrochemical oxidant-and metal-free dehydrogenative coupling of S-H/N-H

A practical and scalable electrochemical oxidation of S-H and N-H was developed. This oxidant- and catalyst-free electrochemical process enables S-N bond formation with inexpensive nickel electrodes in an undivided cell. This procedure exhibits broad substrate scopes and good functional-group compatibility. A 50 g scale oxidative coupling augurs well for industrial applications.

Process for the preparation of thiazolesulphenamides

Thiazolesulphenamides, useful as rubber vulcanization accelerators, are made by reaction of a 2-mercapto-thiazole or a 2,2'-dithiazolyl disulphide with ammonia or a primary or secondary amine in the presence of oxygen and a copper catalyst of specified kind.