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89384-50-9

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89384-50-9 Usage

General Description

D-Alanine, N-methyl-N-(phenylmethyl)- is a chemical compound that is a derivative of the amino acid alanine. It is also known as N-methyl benzyl alanine and is used in the synthesis of peptides and proteins. D-Alanine, N-methyl-N-(phenylmethyl)- is a chiral molecule that is commonly used in the production of pharmaceutical drugs and biologically active compounds. It is a white crystalline powder that is sparingly soluble in water and has a molecular weight of 177.23 g/mol. D-Alanine, N-methyl-N-(phenylmethyl)- is widely used in the pharmaceutical industry and in research laboratories for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 89384-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,8 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89384-50:
(7*8)+(6*9)+(5*3)+(4*8)+(3*4)+(2*5)+(1*0)=179
179 % 10 = 9
So 89384-50-9 is a valid CAS Registry Number.

89384-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-N-methyl-N-benzyl-(R)-Ala

1.2 Other means of identification

Product number -
Other names (R)-N-Benzyl-N-methylalanin

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:89384-50-9 SDS

89384-50-9Relevant articles and documents

Amino Acids, 4 - Enantioselective Synthesis of N-Substituted α-Amino Carboxylic Acids from α-Hydroxy Carboxylic Acids

Effenberger, Franz,Burkard, Ulrike,Willfahrt, Joachim

, p. 314 - 333 (2007/10/02)

With primary and secondary amines, the (S)-α-(trifluoromethylsulfonyloxy) carboxylates (S)-3 afford in an SN2 reaction the N-substituted (R)-α-amino carboxylates (R)-5, (R)-9, and (R)-12, resp.The rates of α-substituted ethyl propionates decrease in the order of the substituents triflate (3a) >> bromide (8a) > mesylate (7a) >= tosylate (7b) > chloride (8b); in the reactions with amines, decreasing reactivity affords increasing racemisation and elimination as a consequence of the more drastic conditions which are required

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