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10567-73-4

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10567-73-4 Usage

General Description

O-MONO-2,4-DNP-L-TYROSINE is a synthetic chemical compound that is a derivative of the amino acid tyrosine. It is often used in research and pharmaceutical applications as a building block for the synthesis of various drugs and compounds. The compound contains a dinitrophenyl (DNP) group, which imparts unique properties and reactivity to the molecule. O-MONO-2,4-DNP-L-TYROSINE has been studied for its potential applications in drug delivery systems and as a chemical probe for studying biological processes. Its specific properties and potential uses make it a valuable tool for researchers and pharmaceutical developers.

Check Digit Verification of cas no

The CAS Registry Mumber 10567-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,6 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10567-73:
(7*1)+(6*0)+(5*5)+(4*6)+(3*7)+(2*7)+(1*3)=94
94 % 10 = 4
So 10567-73-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H13N3O7/c16-12(15(19)20)7-9-1-4-11(5-2-9)25-14-6-3-10(17(21)22)8-13(14)18(23)24/h1-6,8,12H,7,16H2,(H,19,20)

10567-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-3-[4-(2,4-dinitrophenoxy)phenyl]propanoic acid

1.2 Other means of identification

Product number -
Other names O-<2,4-Dinitro-phenyl>-L-tyrosin

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:10567-73-4 SDS

10567-73-4Relevant articles and documents

Enantiomeric Selectivity in the Reactions of Natural Amino Acids with 1-Fluoro-2,4-dinitrobenzene in the Presence of Cyclodextrins

Barra, Monica,Rossi, Rita H. de

, p. 5020 - 5025 (2007/10/02)

The reactions of 1-fluoro-2,4-dinitrobenzene with both enantiomers of the α-amino acids alanine (2a), methionine (2b), valine (2c), leucine (2d), tyrosine (2e), phenylalanine (2f), and tryptophan (2g) were studied in the presence of β-cyclodextrin (β-CD).

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