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116912-15-3

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116912-15-3 Usage

General Description

L-Leucine, N-[N-(phenylacetyl)-L-phenylalanyl]-, 2-propenyl ester is a chemical compound that is a derivative of L-leucine and L-phenylalanine. It is commonly used in the field of medicinal chemistry for its potential biological activity, including its ability to act as a protease inhibitor. L-Leucine, N-[N-(phenylacetyl)-L-phenylalanyl]-, 2-propenyl ester is also being studied for its potential as a therapeutic agent for various conditions, such as cancer and neurodegenerative diseases. Additionally, it may also have applications in the field of drug delivery and development. Overall, L-Leucine, N-[N-(phenylacetyl)-L-phenylalanyl]-, 2-propenyl ester is a versatile chemical compound with promising potential in various areas of research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 116912-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,9,1 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116912-15:
(8*1)+(7*1)+(6*6)+(5*9)+(4*1)+(3*2)+(2*1)+(1*5)=113
113 % 10 = 3
So 116912-15-3 is a valid CAS Registry Number.

116912-15-3SDS

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 N-(Phenylacetyl)-L-phenylalanyl-L-leucin-allylester

1.2 Other means of identification

Product number -
Other names (S)-4-Methyl-2-((S)-3-phenyl-2-phenylacetylamino-propionylamino)-pentanoic acid allyl 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:116912-15-3 SDS

116912-15-3Relevant articles and documents

The Phenylacetyl (PhAc) Group as Enzymatically Removable Protecting Function for Peptides and Carbohydrates: Selective Deprotections with Penicillin Acylase

Waldmann, Herbert

, p. 1175 - 1180 (2007/10/02)

Using the modified carbodiimide procedure or EEDQ as coupling reagent, N-Phenylacetyl (PhAc) amino acids are condensed in good yields with amino acid methyl, benzyl, allyl, and tert-butyl esters to give totally protected dipeptides.The PhAc group is stabl

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