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119906-14-8

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119906-14-8 Usage

Description

D-Alanine, 3-[(phenylmethyl)amino]is a unique chemical compound that features the amino acid D-alanine linked to a phenylmethylamine group. D-Alanine, 3-[(phenylmethyl)amino]combines the essential role of D-alanine in protein synthesis within the human body with the presence of phenylmethylamine, a substance found across the plant and animal kingdoms. Its distinctive structure endows it with a range of biological and pharmacological properties, making it a subject of interest for research into potential therapeutic applications for various medical conditions.

Uses

Used in Pharmaceutical Development:
D-Alanine, 3-[(phenylmethyl)amino]is utilized as a pharmaceutical agent for its potential role in the treatment of specific medical conditions. Its unique structure allows it to interact with biological systems in ways that may offer therapeutic benefits, although further research is necessary to fully understand and harness its potential.
Used in Research Applications:
In the field of scientific research, D-Alanine, 3-[(phenylmethyl)amino]serves as a valuable compound for studying the effects of amino acid derivatives on biological systems. It can be used to investigate the mechanisms of protein synthesis, the influence of phenylmethylamine on various physiological processes, and to explore new avenues for drug discovery.
Used in Nutraceutical Formulations:
Given its status as a derivative of an essential amino acid, D-Alanine, 3-[(phenylmethyl)amino]may also find use in the development of nutraceutical products aimed at supporting health and well-being. Its incorporation into dietary supplements could potentially offer benefits related to protein synthesis and overall health maintenance.

Check Digit Verification of cas no

The CAS Registry Mumber 119906-14-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,9,0 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119906-14:
(8*1)+(7*1)+(6*9)+(5*9)+(4*0)+(3*6)+(2*1)+(1*4)=138
138 % 10 = 8
So 119906-14-8 is a valid CAS Registry Number.

119906-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-amino-3-(benzylamino)propanoic acid

1.2 Other means of identification

Product number -
Other names -

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:119906-14-8 SDS

119906-14-8Upstream product

119906-14-8Downstream Products

119906-14-8Relevant articles and documents

ASYMMERTIC SYNTHESIS OF Β-SUBSTITUTED α-AMINO ACIDS VIA A CHIRAL Ni(II) COMPLEX OF DEHYDROALANINE

Belokon, , Yuri N.,Sagyan, Ashot S.,Djamgaryan, Silva M.,Bakhmutov, Vladimir I.,Belikov, Vasili M.

, p. 5507 - 5514 (2007/10/02)

An efficient approach to the asymmetric synthesis of β-substituted (S)-alanines is describen.The chiral Ni(II) complex of a Schiff base derived from (S)-o-N-(N-benzylpropyl)aminobenzophenone (BBP) and glycine was treated with formaldehyde and sodium methoxide to give a corresponding (R)-serine complex which, in turn, was converted to the chiral Ni(II) dehydroalanine complex.Michael type base catalyzed addition of nucleophiles (including MeOH, Me2NH, PhCH2NH2, imidazole, PhSH, PhCH2SH,, malonic ester and benzylmagnesium chloride) produced a mixture of diastereoisomeric complexes with a 70-90percent excess of S,S (or L,L) isomers over the S,R (or L,D) ones.The cleavage of pure diastereoisomers with aqueous HCl gave, in good yields, β-substituted (S) (or L)-alanines and regenerated the chiral auxiliary (BBP).

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