215391-92-7

Basic information

• Product Name: 4-(benzylamino)-1-phenylbutan-1-ol
• Synonyms: 4-(benzylamino)-1-phenylbutan-1-ol
• CAS NO: 215391-92-7
• Molecular Weight: 255.36
• Mol File: 215391-92-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-(benzylamino)-1-phenylbutan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(benzylamino)-1-phenylbutan-1-ol(215391-92-7)
• EPA Substance Registry System: 4-(benzylamino)-1-phenylbutan-1-ol(215391-92-7)

Safety Data

• Hazardous Substances Data: 215391-92-7(Hazardous Substances Data)

Upstream product

• 33553-82-1 4-chloro-1-phenyl-1-butanol 
• 100-46-9 benzylamine 
• 2243-53-0 trans-styrylacetic acid 
• 93652-37-0 4-phenyl-3-butenyl para-toluenesulfonate 
• 1039627-10-5 (E)-N-benzyl-4-phenylbut-3-en-1-amine 
• 939-52-6 4-chloro-1-phenylbutan-1-one 
• 7510-08-9 N-benzyl-4-oxo-4-phenylbutanamide 
• 62050-98-0 N-benzyl-4-hydroxy-4-phenylbutanamide 
• 1008-76-0 4,5-dihydro-5-phenyl-2(3H)-furanone 

Downstream Products

• 215391-93-8 2-[Benzyl-(4-hydroxy-4-phenyl-butyl)-amino]-1-phenyl-ethanone 

Relevant articles and documents

THIOETHER TRIAZOLOPYRIDINE AND TRIAZOLOPYRMIDINE INHIBITORS OF MYELOPEROXIDASE

The present invention provides compounds of Formula (I):wherein A, X and Y are as defined in the specification, and compositions comprising any of such novel compounds. These compounds are myeloperoxidase (MPO) inhibitors and/or eosinophil peroxidase (EPX) inhibitors, which may be used as medicaments.

A mechanistic alternative for the intramolecular hydroboration of homoallylic amine and phosphine borane complexes

Intramolecular hydroboration is demonstrated starting from homoallylic amine boranes upon activation by iodine. The process involves a B-iodoborane complex as the intermediate and may occur via internal displacement of iodide by the alkene to generate a cationic borane-alkene π-complex on the way to hydroboration products. The reaction can be carried out using a catalytic amount of iodine. Copyright