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L-Valinamide, N-[(phenylmethoxy)carbonyl]-L-phenylalanyl-N-(2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51163-93-0

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51163-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51163-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,6 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51163-93:
(7*5)+(6*1)+(5*1)+(4*6)+(3*3)+(2*9)+(1*3)=100
100 % 10 = 0
So 51163-93-0 is a valid CAS Registry Number.

51163-93-0SDS

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 Z-Phe-Val-o-nitroanilid

1.2 Other means of identification

Product number -
Other names {(S)-1-[(S)-2-Methyl-1-(2-nitro-phenylcarbamoyl)-propylcarbamoyl]-2-phenyl-ethyl}-carbamic acid benzyl ester

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:51163-93-0 SDS

51163-93-0Downstream Products

51163-93-0Relevant academic research and scientific papers

A remarkable catalytic effect of the potassium salt of 1-hydroxybenzotriazole on peptide bond formation

Horiki, Kusuo,Murakami, Atsuko

, p. 615 - 622 (2007/10/02)

A semiquantitative investigation was done on the catalytic effects of 1-hydroxybenzotriazole (HOBt) (5) and the potassium salt 6 of HOBt (5) on peptide bond formation by the active ester method. HOBt (5) was found to catalyze the aminolysis reaction of two different types of active esters, benzyloxy-carbonyl-l-phenylalanine 2,4,5-trichlorophenyl ester (1) and benzyloxycarbonyl-l-phenylalanine 1-succinimidyl ester (2), in tetrahydrofuran (THF) and in a dipolar aprotic dimethylformamide (DMF) solvent. A large rate enhancement was also observed in the aminolysis reaction of 1 in THF when the potassium salt 6 of HOBt (5) was added in the presence of dicyclohexyl-18-crown-6 (7). The rate acceleration in the aminolysis reaction of the active esters by 5 and 6 may reasonably be explained in terms of nucleophilic catalysis.

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