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L-Alanine, N-[(2-hydroxyphenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57471-91-7

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57471-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57471-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,7 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57471-91:
(7*5)+(6*7)+(5*4)+(4*7)+(3*1)+(2*9)+(1*1)=147
147 % 10 = 7
So 57471-91-7 is a valid CAS Registry Number.

57471-91-7SDS

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 N-(2-hydroxybenzyl)-L-α-alanine

1.2 Other means of identification

Product number -
Other names 2-hydroxybenzyl-Ala

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:57471-91-7 SDS

57471-91-7Downstream Products

57471-91-7Relevant academic research and scientific papers

Chiral metal-organic frameworks for high-resolution gas chromatographic separations

Xie, Sheng-Ming,Zhang, Ze-Jun,Wang, Zhi-Yu,Yuan, Li-Ming

, p. 11892 - 11895 (2011)

Chiral metal-organic framework coated open tubular columns are used in the high-resolution gas chromatographic separation of chiral compounds. The columns have excellent selectivity and also possess good recognition ability toward a wide range of organic

The N-(2-hydroxybenzyl) protecting group for amide bond protection in solid phase peptide synthesis

Johnson, Tony,Quibell, Martin

, p. 463 - 466 (1994)

Backbone amide protection using the N-(2-hydroxybenzyl) group to overcome chain aggregation during solid phase peptide synthesis is described. This is illustrated by the preparation of the notoriously difficult decapeptide acyl carrier protein (65-74). Th

Amino acid derivatives and active oxygen-resisting agent

-

, (2008/06/13)

Provided is a novel active oxygen-resisting agent which has an excellent active oxygen resistance and which exhibits a good solubility in an oil solvent. An active oxygen-resisting agent containing as an active ingredient an amino acid derivative represented by the following formula (I) STR1 wherein Ar represents a substituted or substituted 2-hydroxyphenyl group or a pyridyl group, said substitution being selected from the group consisting of a halogen atom, a C1-6 alkyl group, a hydroxyl group, a hydroxy C1-6 alkyl group, a nitro group, a C1-6 alkoxyl group or a carboxyl group, R1 represents a side chain of an amino acid, X represents --O-- or --NH--, R2 represents a C8-22 alkyl group, and n represents 0 or 1, or its salt.

Topochemical conversion of a hydrogen-bonded three-dimensional network into a covalently bonded framework

Ranford, John D.,Vittal, Jagadese J.,Wu, Daqing

, p. 1114 - 1116 (2007/10/03)

Thermal dehydration promotes the topochemical conversion of the hydrogen-bonded dimeric complex [{Zn(sala)(H2O)2}2]·2H2O (H2-(sala) = N-(2-hydroxybenzyl)-L-alanine) to generate covalent [{Zn(sala)}(n)

ASSESSING THE EFFECT OF LIGAND PROXIMITY ON CHIROPTICAL AND OTHER PROPERTIES IN COBALT(III) MODEL, TYROSINE-LIKE COMPLEXES

Jursik, Frantisek,Archer, Ronald, D.

, p. 2097 - 2106 (2007/10/03)

A series of new cobalt(III) octahedral complexis of the general formula Na (ohb-aa=N-(o-hydroxybenzyl)amino acid anion; amino acid= glycine, (S)-α-alanine, α-aminoisobutyric acid, (S)-valine, (S)-norvaline and (S)-leucine) were prepared by th

REACTION OF TRIFLUOROACETIC ANHYDRIDE WITH N-(2-HYDROXYBENZYL)-α-AMINO ACIDS: AN ENTRY IN THE NEW OXAZOLOBENZOXAZINE RING SYSTEM

Chantegrel, Bernard,Deshayes, Christian,Faure, Rene

, p. 2811 - 2818 (2007/10/02)

The diastereospecific double ring closure of N-(2-hydroxybenzyl)-α-amino acids with trifluoroacetic anhydride leads to the formation of 10a-trifluoromethyl-2,3,4,10a-tetrahydro-oxazolobenzoxazin-2(5H)-ones.The chemical structures are supp

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