60509-42-4

Basic information

• Product Name: N-(2-METHYLBENZYL)BUTAN-1-AMINE
• Synonyms: CHEMBRDG-BB 9070535;N-(2-METHYLBENZYL)BUTAN-1-AMINE;AKOS LT-1098X1403;N-(2-METHYLBENZYL)-1-BUTANAMINE;N-(2-METHYLPHENYLMETHYL)BUTYLAMINE;UKRORGSYN-BB BBV-125499;N-(2-methylbenzyl)-1-butanamine(SALTDATA: HCl)
• CAS NO: 60509-42-4
• Molecular Formula: C₁₂H₁₉N
• Molecular Weight: 177.29
• Mol File: 60509-42-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 255.7°C at 760 mmHg
• Flash Point: 104.8°C
• Appearance: /
• Density: 0.9g/cm³
• Vapor Pressure: 0.0161mmHg at 25°C
• Refractive Index: 1.502
• CAS DataBase Reference: N-(2-METHYLBENZYL)BUTAN-1-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-METHYLBENZYL)BUTAN-1-AMINE(60509-42-4)
• EPA Substance Registry System: N-(2-METHYLBENZYL)BUTAN-1-AMINE(60509-42-4)

Safety Data

• Hazardous Substances Data: 60509-42-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H19N/c1-3-4-9-13-10-12-8-6-5-7-11(12)2/h5-8,13H,3-4,9-10H2,1-2H3

Upstream product

• 152126-84-6 N-(2-methylbenzylidene)butan-1-amine 
• 529-20-4 2-methylphenyl aldehyde 

Relevant articles and documents

First efficient two-step/one-pot zirconium (IV)isopropoxide-mediated reductive amination of carbonyl compounds

An efficient method for the synthesis of various primary and secondary amines through a zirconium(IV) isopropoxide-mediated reductive amination reaction of aldehydes and ketones is reported. A series of different aldehydes, ketones and amines were used leading to the expected amino products in moderate to excellent yields. The mechanistic rationale of this reaction has been postulated through the formation of a transient imine species and a diastereoselective version using (R)-phenylethylamine as chiral inducer led to the expected products in moderate to excellent yields and with diastereoselectivities up to 100%.