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2-(benzyloxy)propan-1-amine, also known as 1-(2-aminopropyl)benzene, is a chemical compound with the molecular formula C10H15NO. It is a secondary amine featuring a benzyl group attached to the oxygen atom, which is commonly utilized in organic synthesis as a building block for the creation of various pharmacologically active compounds.

6449-46-3

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6449-46-3 Usage

Uses

Used in Pharmaceutical Industry:
2-(benzyloxy)propan-1-amine is used as a key intermediate in the synthesis of antidepressants, antihistamines, and other therapeutic drugs, contributing to the development of medications that address a range of health conditions.
Used in Research Laboratories:
In research settings, 2-(benzyloxy)propan-1-amine serves as a reagent for the production of novel chemical compounds, facilitating scientific exploration and innovation in the field of chemistry and related disciplines.

Check Digit Verification of cas no

The CAS Registry Mumber 6449-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,4 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6449-46:
(6*6)+(5*4)+(4*4)+(3*9)+(2*4)+(1*6)=113
113 % 10 = 3
So 6449-46-3 is a valid CAS Registry Number.

6449-46-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylmethoxypropan-1-amine

1.2 Other means of identification

Product number -
Other names (+-)-1-Amino-2-benzyloxy-propan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6449-46-3 SDS

6449-46-3Downstream Products

6449-46-3Relevant academic research and scientific papers

Selective O-benzylation of aminoalkanols

Hu,Cassady

, p. 907 - 913 (2007/10/02)

A simple and one-step method has been developed for selective O-benzylation of aminoalkanols. Study of steric effects shows the best selectivity in adjacent 1°-OH vs 2°-CHNH2 and decreased selectivity in 2°-OH vs 1°-CH2NH2 and non adjacent aminoalkanol.

UTILISATION DU PALLADIUM COMME CATALYSEUR DE N,N-DIDESALLYLATION

Picq, D.,Cottin, M.,Anker, D.,Pacheco, H.

, p. 1399 - 1402 (2007/10/02)

Palladium on charcoal is more efficient than usual catalysts to perform N,N-dideallylation of amines; synthetic applications on aminosugars field using nitrogen atom transfer in a one pot reaction are described.

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