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124613-28-1

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124613-28-1 Usage

General Description

2-(benzylamino)propane-1,3-diol is a chemical compound with the molecular formula C10H15NO2. It is a secondary amine derivative of propane-1,3-diol that contains a benzyl group. 2-(benzylamino)propane-1,3-diol has potential applications in the pharmaceutical and chemical industries. It can be used in the synthesis of various drugs and as a building block in the production of other organic compounds. Additionally, it may have potential uses as a chiral reagent in asymmetric synthesis. However, it is important to handle and use this chemical with care, as it may have potential health hazards and environmental impacts if not managed properly.

Check Digit Verification of cas no

The CAS Registry Mumber 124613-28-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,6,1 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124613-28:
(8*1)+(7*2)+(6*4)+(5*6)+(4*1)+(3*3)+(2*2)+(1*8)=101
101 % 10 = 1
So 124613-28-1 is a valid CAS Registry Number.

124613-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 1,3-Propanediol,2-[(phenylmethyl)amino]

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:124613-28-1 SDS

124613-28-1Relevant articles and documents

An oxazetidine amino acid for chemical protein synthesis by rapid, serine-forming ligations

Pusterla, Ivano,Bode, Jeffrey W.

, p. 668 - 672 (2015)

Amide-forming ligation reactions allow the chemical synthesis of proteins by the union of unprotected peptide segments, and enable the preparation of protein derivatives not accessible by expression or bioengineering approaches. The native chemical ligati

Carbonyl-inserted organo-hybrids of a Dawson-type phosphovanadotungstate: Scope and chemoselective oxidation catalysis

Oble, Julie,Riflade, Benoit,Noel, Amandine,Malacria, Max,Thorimbert, Serge,Hasenknopf, Bernold,Lacote, Emmanuel

, p. 5990 - 5993 (2012/01/03)

The Dawson-type polyoxometalate (POM) [P2V3W 15O62]9- is a prototype for inclusion of carbonyls of amides, ureas, carbamates, and thiocarbamates into polyoxometallic structures. The carbonyl-inserted POMs catalyze the oxidation of sulfides. Chemoselectivity depends primarily on the proton content of the POM, but it is also influenced by the organic substituent.

Unambiguous Synthesis of 3-Aryloxymethylmorpholine Hydrochlorides Without Ring Enlargement Side Reactions

Brown, George R.,Foubister, Alan J.

, p. 1401 - 1403 (2007/10/02)

The unambiguous synthesis of 3-naphthyloxymorpholine hydrochloride appetite suppressants is reportet.Chemoselective reduction of 4-benzyl-5-oxomorpholine-3-carboxylic acid and its derivatives is described under various metal hydride reducing conditions.

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