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146277-47-6

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146277-47-6 Usage

General Description

"(S)-2-Amino-3-(2,4,6-trimethyl-phenyl)-propionic acid is a chemical compound that falls under the category of amino acids and derivatives. (S)-2-AMINO-3-(2,4,6-TRIMETHYL-PHENYL)-PROPIONIC ACID has a molecular weight of 235.307 g/mol. It contains elements like carbon, hydrogen, nitrogen, and oxygen. (S)-2-AMINO-3-(2,4,6-TRIMETHYL-PHENYL)-PROPIONIC ACID is identifiable by its systematic name, (S)-2-Amino-3-(2,4,6-trimethyl-phenyl)-propionic acid, and it is structurally characterized by the presence of an amino group, a carboxyl group, and a trimethylphenyl group. Its usage and effect on human health, environment, and other specific applications largely depends on its concentration and it can be synthesized in the lab under controlled conditions. There are no widely-known trade names or brands for this specific chemical compound. It is predominately used in biochemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 146277-47-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,2,7 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 146277-47:
(8*1)+(7*4)+(6*6)+(5*2)+(4*7)+(3*7)+(2*4)+(1*7)=146
146 % 10 = 6
So 146277-47-6 is a valid CAS Registry Number.

146277-47-6SDS

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 (2S)-2-amino-3-(2,4,6-trimethylphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names L-2,4,6-TRIMETHYLPHENYLALANINE

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:146277-47-6 SDS

146277-47-6Upstream product

146277-47-6Relevant articles and documents

METHOD FOR THE STEREOSELECTIVE PREPARATION OF AMINO ACID DERIVATIVES

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Page/Page column 9, (2010/08/09)

The invention relates to a process for the stereoselective preparation of amino acid derivatives, comprising a hydrogenation reaction of the compound of formula (III), alternatively its enantiomer, wherein R is (C1-C8)-alkyl; followe

Nonapeptide and decapeptide analogs of LHRH, useful as LHRH antagonists

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, (2008/06/13)

Nonapeptide and decapeptide analogs of LHRH which have the formula: STR1 and the pharmaceutically acceptable salts thereof, wherein: X is a D-alanyl residue wherein one hydrogen on C-3 is replaced by:(a) a carbocyclic aryl-containing radical selected from the group consisting of phenyl substituted with three or more straight chain lower alkyl groups, naphthyl, anthryl, fluorenyl, phenanthryl, biphenylyl and benzhydryl; or(b) a saturated carbocyclic radical selected from the group consisting of cyclohexyl substituted with three or more straight chain lower alkyl groups, perhydronaphthyl, perhydrobiphenylyl, perhydro-2,2-diphenylmethyl, and adamantyl; or(c) a heterocyclic aryl containing radical selected from the group consisting of radicals represented by the following structural formulas: STR2 wherein A"" and A'' are independently selected from the group consisting of hydrogen, lower alkyl, chlorine, and bromine, and G is selected from the group consisting of oxygen, nitrogen, and sulfur;A is an aminoacyl residue selected from the group consisting of L-pyroglutamyl, D-pyroglutamyl, N-acyl-L-prolyl, N-acyl-D-prolyl, N-acyl-D-tryptophanyl, N-acyl-D-phenylalanyl, N-acyl-D-p-halophenylalanyl, and N-acyl-X wherein X is as defined previously;B is an amino acyl residue selected from the group consisting of D-phenylalanyl, D-p-halophenylalanyl, 2,2-diphenylglycyl, and X wherein X is as defined previously;C is an amino acyl residue selected from the group consisting of L-tryptophanyl, D-tryptophanyl, D-phenylalanyl and X wherein X is as defined above;E is glycinamide or --NH--R 1, wherein R 1 is lower alkyl, cycloalkyl, fluoro lower alkyl or STR3 wherein R 2 is hydrogen or lower alkyl; are disclosed. These compounds are LHRH antagonists.

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