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L-Leucine, N-(N-glycyl-L-phenylalanyl)-, methyl ester, monohydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84759-64-8

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84759-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84759-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,5 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84759-64:
(7*8)+(6*4)+(5*7)+(4*5)+(3*9)+(2*6)+(1*4)=178
178 % 10 = 8
So 84759-64-8 is a valid CAS Registry Number.

84759-64-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name HCl*H-Gly-L-Phe-L-Leu-OMe

1.2 Other means of identification

Product number -
Other names HCl*Gly-Phe-Leu-OMe

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:84759-64-8 SDS

84759-64-8Relevant academic research and scientific papers

PENTAFLUOROPHENYL DIPHENYLPHOSPHINATE A NEW EFFICIENT COUPLING REAGENT IN PEPTIDE CHEMISTRY

Chen, Shaoqing,Xu, Jiecheng

, p. 6711 - 6714 (2007/10/02)

Pentafluorophenyl diphenylphosphinate was found to be a new efficient coupling reagent for the racemization-free synthesis of peptides.It has been applied in both the solution and the solid phase peptide synthesis.

SYNTHESIS OF CHIRAL OLIGOPEPTIDES BY MEANS OF CATALYTIC ASYMMETRIC HYDROGENATION OF DEHYDROPEPTIDES

Ojima, Iwao,Yoda, Noriko,Yatabe, Momoko,Tanaka, Toshiyuki,Kogure, Tetsuo

, p. 1255 - 1268 (2007/10/02)

Asymmetric hydrogenation of Ac-ΔTyr(Ac)-(S)-Ala-Gly-OMe (6), Ac-ΔTyr(Ac)-(R)-Ala-Gly-(S)-Phe-OMe (7), Ac-ΔPhe-NH-CH(R)-CH2-OCH2Ph (10), HCO-ΔPhe-(S)-Leu-OMe (16), X-AA-ΔPhe-AA'-OMe ( 5: X=tBOC, CBZ, CF3CO; AA, AA'= α-amino acid ), and t

SYNTHESIS OF ENKEPHALIN ANALOGS VIA ASYMMETRIC HYDROGENATION OF DEHYDROPEPTIDE BUILDING BLOCKS

Ojima, Iwao,Yoda, Noriko,Yatabe, Momoko

, p. 3917 - 3920 (2007/10/02)

1, D-Ala2, Leu5-OMe>Enkephalin and 1, D-Ala2, Leu5-OMe>Enkephalin were succesfully synthesized by the coupling of dipeptide units and tripeptide units which were readily obt

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