32997-27-6

Basic information

• Product Name: N-(1,3-benzothiazol-2-ylsulfanyl)butan-1-amine
• Synonyms: 2-benzothiazolesulfenamide, N-butyl-; N-(1,3-Benzothiazol-2-ylsulfanyl)-1-butanamine
• CAS NO: 32997-27-6
• Molecular Formula: C₁₁H₁₄N₂S₂
• Molecular Weight: 238.3723
• Mol File: 32997-27-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 358.5°C at 760 mmHg
• Flash Point: 170.6°C
• Density: 1.22g/cm³
• Vapor Pressure: 2.54E-05mmHg at 25°C
• Refractive Index: 1.644
• CAS DataBase Reference: N-(1,3-benzothiazol-2-ylsulfanyl)butan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1,3-benzothiazol-2-ylsulfanyl)butan-1-amine(32997-27-6)
• EPA Substance Registry System: N-(1,3-benzothiazol-2-ylsulfanyl)butan-1-amine(32997-27-6)

Safety Data

• Hazardous Substances Data: 32997-27-6(Hazardous Substances Data)

Upstream product

• 2492-26-4 sodium 2-mercaptobenzothiazole 
• 109-73-9 N-butylamine 
• 149-30-4 2-Mercaptobenzothiazole 
• 2801-21-0 benzothiazole sulfenamide 

Downstream Products

• 120-78-5 di(benzothiazol-2-yl)disulfide 
• 109-73-9 N-butylamine 
• 615-22-5 2-methylmercaptobenzothiazole 
• 20465-01-4 N-butyl-O,O-dimethylphosphoramidate 

Relevant articles and documents

The aqueous phase is generated in the catalytic molecular oxygen with S - N key of the sulfenamide compounds (by machine translation)

The invention provides a water-phase catalytic molecular oxygen generation has S - N key of the sulfenamide compounds, in order to water-soluble transition metal phthalocyanine compound as a catalyst, in oxygen or in the air environment, the mercapto comp

MECHANISM OF THE REACTIONS OF 2-BENZOTHIAZOLESULFENAMIDES WITH NUCLEOPHILIC REAGENTS

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