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73942-36-6

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73942-36-6 Usage

General Description

AC-D-PHE-TYR-OH is a chemical compound consisting of the amino acids D-phenylalanine and tyrosine linked by a peptide bond. It is a dipeptide with a molecular formula of C20H23N3O4. Dipeptides are important building blocks of proteins and can also have potential applications in the pharmaceutical industry due to their bioactive properties. AC-D-PHE-TYR-OH is a synthetic compound commonly used in research and drug development due to its ability to mimic natural biological systems and have potential therapeutic effects. It has been studied for its role in various biological processes and its potential as a drug candidate for conditions such as cancer and neurodegenerative diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 73942-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,4 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73942-36:
(7*7)+(6*3)+(5*9)+(4*4)+(3*2)+(2*3)+(1*6)=146
146 % 10 = 6
So 73942-36-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H22N2O5/c1-13(23)21-17(11-14-5-3-2-4-6-14)19(25)22-18(20(26)27)12-15-7-9-16(24)10-8-15/h2-10,17-18,24H,11-12H2,1H3,(H,21,23)(H,22,25)(H,26,27)/t17-,18?/m1/s1

73942-36-6SDS

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 (2R)-2-acetamido-3-phenylpropanoic acid,(2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names N-ACETYL-D-PHENYLALANINE-TYROSINE

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:73942-36-6 SDS

73942-36-6Upstream product

73942-36-6Downstream Products

73942-36-6Relevant articles and documents

Asymmetric hydrogenation of N-acetylhydrodipeptide complexes with Mg(II) and C(II) ions

Lisichkina, I. N.,Vinogradova, A. I.,Sukhorukova, N. B.,Tselyapina, E. V.,Saporovskaya, M. B.,Belikov, V. M.

, p. 569 - 571 (2007/10/02)

N-Ac-Δ-Phe-AA form labile complexes with Mg(II) ions.Potentiometric titration data show that the carboxyl group of the dehydropeptide in them scarcely participates in complexation, unlike the complexes with Ca(II) ions.The hydrogenation of these complexes

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