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L-Valine, N-[N-[N-[N-(N-acetyl-L-a-glutamyl)-L-alanyl]-L-tyrosyl]-L-leucyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82748-45-6

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82748-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82748-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,4 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82748-45:
(7*8)+(6*2)+(5*7)+(4*4)+(3*8)+(2*4)+(1*5)=156
156 % 10 = 6
So 82748-45-6 is a valid CAS Registry Number.

82748-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ac-Glu-Ala-Tyr-Leu-Val-OH

1.2 Other means of identification

Product number -
Other names (S)-2-{(S)-2-[(S)-2-[(S)-2-((S)-2-Acetylamino-4-carboxy-butyrylamino)-propionylamino]-3-(4-hydroxy-phenyl)-propionylamino]-4-methyl-pentanoylamino}-3-methyl-butyric acid

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:82748-45-6 SDS

82748-45-6Downstream Products

82748-45-6Relevant articles and documents

SOLID PHASE SYNTHESIS OF TYROSINE-CONTAINING HISTONE FRAGMENTS

Giralt, Ernest,Andreu, David,Miro, Pere,Pedroso, Enrique

, p. 3185 - 3188 (1983)

The solid phase synthesis of Ac-Val-Val-Tyr-Ala-Leu-OH (1), Ac-Glu-Ala-Tyr-Leu-Val-OH (2) and Ac-Leu-Tyr-Gly-Phe-Gly-Gly-OH (3), segments 86-90 of histone H4, 97-101 of histone H3 and 97-102 of histone H4, respectively, is described using chloromethylresin and chloromethyl-Pab-resin as solid supports.In the synthesis of peptides 2 and 3 using 2,6-dichlorobenzyl ether as tyrosine side chain protection, 7percent and 8percent of the 3-dichlorobenzyltyrosine-rearranged peptide could be isolated by Bio-Gel P-2 or diethylaminoethylcellulose chromatography.Alternative use of cyclohexyl ether as tyrosine protection has been explored with satisfactory results.

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