156143-26-9

Basic information

• Product Name: N-methyltropan-3-yl 2-(4-bromophenyl)propionate
• Synonyms: N-methyltropan-3-yl 2-(4-bromophenyl)propionate
• CAS NO: 156143-26-9
• Molecular Formula: C17H22 Br N O2
• Molecular Weight: 352.27
• Mol File: 156143-26-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 414.4°Cat760mmHg
• Flash Point: 204.4°C
• Appearance: /
• Density: 1.36g/cm³
• Vapor Pressure: 4.48E-07mmHg at 25°C
• Refractive Index: 1.589
• CAS DataBase Reference: N-methyltropan-3-yl 2-(4-bromophenyl)propionate(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyltropan-3-yl 2-(4-bromophenyl)propionate(156143-26-9)
• EPA Substance Registry System: N-methyltropan-3-yl 2-(4-bromophenyl)propionate(156143-26-9)

Safety Data

• Hazardous Substances Data: 156143-26-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H22BrNO2/c1-11(12-3-5-13(18)6-4-12)17(20)21-16-9-14-7-8-15(10-16)19(14)2/h3-6,11,14-16H,7-10H2,1-2H3

Upstream product

• 156143-00-9 (S)-(+)-2-(4'-bromophenyl)propanoic acid 
• 42186-06-1 2-(4-Bromophenyl)propionitrile 
• 7432-10-2 Tropanol 
• 156142-98-2 (R)-(-)-2-(4'-bromophenyl)propanoic acid 
• 362061-49-2 (R)-(-)-2-(4'-bromophenyl)propionamide 
• 53086-53-6 2-(4-bromophenyl)propionic acid 
• 185756-11-0 α-methyl 4-bromophenylacetyl chloride 
• 120-29-6 3-tropanol 

Relevant articles and documents

Enantioselective hydrolysis of various racemic α-substituted arylacetonitriles using Rhodococcus sp. CGMCC 0497

The enantioselective hydrolysis of 17 racemic α-substituted arylacetonitriles by Rhodococcus sp. CGMCC 0497 is described. The corresponding (R)-amides and (S)-acids were obtained with excellent enantiomeric excess in most cases. The effect of steric and electronic factors on the outcome of the reactions are discussed here. The results prove that nitrile-converting enzymes are efficient tools for the synthesis of sterically unencumbered chiral α-arylpropionic acids and amides.