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124491-96-9

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124491-96-9 Usage

General Description

N~1~,N~1~-dimethylalaninamide, also known as 1HCl 0.01C6H4(COOH)2, is a chemical compound with the molecular formula C6H11N2O. It is commonly used as an organic intermediate in the synthesis of pharmaceuticals and other organic compounds. This chemical is also known for its use in various biochemical research applications. The presence of the hydrochloride salt (1HCl) and benzoic acid (0.01C6H4(COOH)2) in the compound's name suggests that it may have potential pharmaceutical or medicinal applications. However, further research and studies would be needed to fully understand the properties and potential uses of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 124491-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,9 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124491-96:
(8*1)+(7*2)+(6*4)+(5*4)+(4*9)+(3*1)+(2*9)+(1*6)=129
129 % 10 = 9
So 124491-96-9 is a valid CAS Registry Number.

124491-96-9SDS

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-Amino-N,N-dimethylpropanamide hydrochloride

1.2 Other means of identification

Product number -
Other names (RS)-alanine N,N-dimethylamide

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:124491-96-9 SDS

124491-96-9Relevant articles and documents

Enantioselection in peptide bond formation

Hill, Roger R.,Birch, David,Jeffs, Graham E.,North, Michael

, p. 965 - 972 (2007/10/03)

Selectivity in abiotic condensations of amino acids remains controversial and stereochemically little explored. We find that competitive activated couplings of N-acyl derivatives of glycine, alanine, valine, proline and phenylalanine with binary, ternary and quaternary mixtures of amides and esters of the same group of amino acids show little selectivity among the reactants, except with respect to configuration, where a consistent and significant preference for heterochiral outcomes, mostly >80%, is observed. One possible explanation of this selectivity predicts a predisposition to homochiral coupling under conditions that would require the two carboxyl functions to be co-facial in the activated complex.

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