210096-61-0

Basic information

• Product Name: N-(4-hydroxybutyl)benzothioamide
• Synonyms: N-(4-hydroxybutyl)benzothioamide
• CAS NO: 210096-61-0
• Molecular Weight: 209.312
• Mol File: 210096-61-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(4-hydroxybutyl)benzothioamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-hydroxybutyl)benzothioamide(210096-61-0)
• EPA Substance Registry System: N-(4-hydroxybutyl)benzothioamide(210096-61-0)

Safety Data

• Hazardous Substances Data: 210096-61-0(Hazardous Substances Data)

Upstream product

• 13325-10-5 4-Aminobutanol 
• 100-46-9 benzylamine 
• 210096-63-2 N-[4-(tert-Butyl-dimethyl-silanyloxy)-butyl]-benzamide 
• 98-88-4 benzoyl chloride 
• 102877-79-2 N-(4-hydroxybutyl)benzamide 
• 210096-64-3 N-[4-(tert-Butyl-dimethyl-silanyloxy)-butyl]-thiobenzamide 

Downstream Products

• 15563-45-8 1-thiobenzoylpyrrolidine 
• 10554-32-2 2-phenyl-4,5,6,7-tetrahydro-1,3-thiazepine 

Relevant articles and documents

Microwave-assisted synthesis of 2-substituted 4,5,6,7-tetrahydro-1,3-thiazepines from 4-aminobutanol

A general procedure for the synthesis of 2-substituted tetrahydro-1,3-thiazepines by MW-assisted cyclization of 4-thioamidobutanols is presented. The acyclic precursors were prepared in high overall yields by an expeditious three-step diacylation/thionati

Synthesis of oxazines and thiazines by cyclodehydration of hydroxy amides and thioamides

Dihydro-1,3-oxazines and -thiazines were obtained by cyclodehydration of hydroxy amides and thioamides with PEG-linked Burgess reagent or under Mitsunobu conditions. Yields were generally higher with polymer-Burgess reagent, but both conditions failed to