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7462-56-8

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7462-56-8 Usage

Compound class

Primary amines, which are organic compounds containing a primary amine group.

Physical state

A clear, colorless liquid.

Molecular weight

197.27 g/mol.

Uses

Commonly used in the pharmaceutical and research industries as a building block in the synthesis of various pharmaceutical drugs and organic compounds.

Chemical reactivity

Its primary amine group allows it to participate in a variety of chemical reactions, making it a versatile intermediate in the production of a wide range of compounds.

Biological activity

Known to have various biological activities and can act as a chelating agent, making it potentially useful in medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7462-56-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7462-56:
(6*7)+(5*4)+(4*6)+(3*2)+(2*5)+(1*6)=108
108 % 10 = 8
So 7462-56-8 is a valid CAS Registry Number.

7462-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzylamino)butane-1,3-diol

1.2 Other means of identification

Product number -
Other names N-Benzyl-DL-allothreoninol

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:7462-56-8 SDS

7462-56-8Relevant articles and documents

Regioselective ring opening of chiral epoxyalcohols by primary amines

Canas, Marc,Poch, Marta,Verdaguer, Xavier,Moyano, Albert,Pericas, Miquel A.,Riera, Antoni

, p. 6931 - 6934 (2007/10/02)

A reinvestigation of the titanium(IV)-mediated reaction of primary amines with chiral 2,3-epoxyalcohols shows that, contrary to previous reports, this reaction constitutes a general and practical process for the enantioselective synthesis of 3-amino-1,2-diols.

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