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CARBOBENZYLOXY-L-ALANYL-L-LEUCINE BENZYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51021-85-3

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51021-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51021-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,2 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51021-85:
(7*5)+(6*1)+(5*0)+(4*2)+(3*1)+(2*8)+(1*5)=73
73 % 10 = 3
So 51021-85-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H30N2O5/c1-17(2)14-21(23(28)30-15-19-10-6-4-7-11-19)26-22(27)18(3)25-24(29)31-16-20-12-8-5-9-13-20/h4-13,17-18,21H,14-16H2,1-3H3,(H,25,29)(H,26,27)

51021-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 4-methyl-2-[2-(phenylmethoxycarbonylamino)propanoylamino]pentanoate

1.2 Other means of identification

Product number -
Other names Z-Ala-Leu-OBn

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:51021-85-3 SDS

51021-85-3Upstream product

51021-85-3Downstream Products

51021-85-3Relevant academic research and scientific papers

A method for cleaving an allyl protecting group at the amide nitrogen of peptides by one-pot olefin isomerization-oxidation

Kajihara, Kouki,Arisawa, Mitsuhiro,Shuto, Satoshi

supporting information; experimental part, p. 9494 - 9496 (2009/04/06)

(Chemical Equation Presented) A facile method for N-deallylation at the amide nitrogen of peptides is described. One-pot deallylation of a substrate through ruthenium hydride-catalyzed terminal olefin isomerization and subsequent ozonolysis gave the corresponding deallylated product under mild conditions.

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