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25548-16-7

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25548-16-7 Usage

General Description

3-AMINO-4-[(1-BENZYL-2-METHOXY-2-OXOETHYL)AMINO]-4-OXOBUTANOIC ACID is a chemical compound with a complex structure comprising an amino group and a benzyl group. It is classified as a peptide derivative, containing four carbon atoms arranged in a chain with carboxyl and amino groups at either end. The compound also contains a benzyl group attached to a methoxy and oxoethyl functional group, contributing to its unique chemical properties. 3-AMINO-4-[(1-BENZYL-2-METHOXY-2-OXOETHYL)AMINO]-4-OXOBUTANOIC ACID may have potential applications in pharmaceuticals, biochemistry, and organic synthesis due to its specific structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 25548-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,4 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25548-16:
(7*2)+(6*5)+(5*5)+(4*4)+(3*8)+(2*1)+(1*6)=117
117 % 10 = 7
So 25548-16-7 is a valid CAS Registry Number.

25548-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-4-[(1-methoxy-1-oxo-3-phenylpropan-2-yl)amino]-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names D-Asp-L-PheOMe

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:25548-16-7 SDS

25548-16-7Relevant articles and documents

Process for preparing peptides and N-carbamoyl-protected peptides

-

, (2008/06/13)

The invention concerns a process for the enzymatic preparation of protected di- and oligopeptides and the separation of the protective groups used. The process according to the invention enables peptides to be synthesized simply and economically and the protective group to be separated carefully. The process comprises three reaction steps: 1. Preparation of N-carbamoyl amino acid or N-carbamoyl amino acid derivatives; 2. Formation of the peptide bond between the carbamoyl-protected electrophile and nucelophile; and 3. Separation of the carbamoyl-protective group.

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