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19542-44-0

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19542-44-0 Usage

General Description

Z-D-ALA-PHE-OH, also known as Z-D-Ala-Phe-OH or Z-D-alanylphenylalanine, is a synthetic compound that consists of the amino acids D-alanine and phenylalanine linked together in a peptide bond. It is often used as a model peptide in research studies due to its stability and structural resemblance to naturally occurring peptides. Z-D-ALA-PHE-OH has been found to exhibit various biological activities, including antimicrobial properties and inhibition of enzymes such as proteases. It is also used as a building block for the synthesis of peptidomimetic compounds with potential therapeutic applications in drug discovery. Overall, Z-D-ALA-PHE-OH plays a significant role in peptide chemistry and has the potential to contribute to the development of novel pharmaceutical agents.

Check Digit Verification of cas no

The CAS Registry Mumber 19542-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,4 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19542-44:
(7*1)+(6*9)+(5*5)+(4*4)+(3*2)+(2*4)+(1*4)=120
120 % 10 = 0
So 19542-44-0 is a valid CAS Registry Number.

19542-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Z-D-ALA-PHE-OH

1.2 Other means of identification

Product number -
Other names Cbz-D-Ala-L-Phe

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:19542-44-0 SDS

19542-44-0Downstream Products

19542-44-0Relevant articles and documents

A modular approach to cyclic tetrapeptides related to histone deacetylase inhibition: Synthesis of epi-microsporin A

Mukherjee, Jyoti Prasad,Sil, Suman,Chattopadhyay, Shital K.

, p. 739 - 742 (2016)

A short new route to the unusual amino acid component (S)-2-amino-8-oxodecanoic acid (Aoda) of some important HDAC inhibitors has been developed using cross metathesis reaction as the key step. An extension of the study employing grafting of a macrocyclic scaffold through cross metathesis has proved to be highly efficient for the synthesis of an isomer of the cyclic tetrapeptide HDAC inhibitor microsporin.

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