101441-76-3

Basic information

• Product Name: N-phenethylbenzo[b]thiophene-2-carboxamide
• Synonyms: N-phenethylbenzo[b]thiophene-2-carboxamide
• CAS NO: 101441-76-3
• Molecular Weight: 281.378
• Mol File: 101441-76-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-phenethylbenzo[b]thiophene-2-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenethylbenzo[b]thiophene-2-carboxamide(101441-76-3)
• EPA Substance Registry System: N-phenethylbenzo[b]thiophene-2-carboxamide(101441-76-3)

Safety Data

• Hazardous Substances Data: 101441-76-3(Hazardous Substances Data)

Upstream product

• 6314-28-9 benzo[b]thiophene-2-carboxylic acid 
• 64-04-0 phenethylamine 
• 39827-11-7 benzothiophene-2-carboxylic acid chloride 

Relevant articles and documents

Alpha-carbonyl alkenyl ester compound as well as preparation method and application thereof

The invention provides an alpha-carbonyl alkenyl ester compound and a preparation method thereof. The alpha-carbonyl alkenyl ester compound is also used for reacting with primary or secondary amine to prepare an amide compound. Two steps of reactions are combined to develop an amido bond and peptide bond forming method which takes carboxylic acid and amine as starting raw materials and allene ketone as a condensing agent. Meanwhile, the alpha-carbonyl alkenyl ester compound of the alpha-amino acid is used as a polypeptide synthesis building block for solid-phase synthesis of polypeptide. The method is mild in reaction condition, simple to operate and high in yield. Compared with an existing amido bond condensation reagent, allene ketone has the advantages of being easy and convenient to prepare, good in stability, small in molecular weight and free of racemization when alpha-chiral carboxylic acid is activated and the like. The compound is a novel amido bond and peptide bond condensation reagent.