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DNPYR-GLYCINE, also known as 2,4-dinitrophenyl-glycine, is a chemical compound that consists of a glycine molecule conjugated with a 2,4-dinitrophenyl group. Glycine is the simplest amino acid and a fundamental building block of proteins, while the 2,4-dinitrophenyl group is an aromatic compound known for its strong absorption in the ultraviolet region. This conjugation results in a molecule that is often used in biochemical research, particularly in assays to detect the activity of enzymes like proteases, which can cleave the peptide bond. The release of the 2,4-dinitrophenyl group upon enzymatic action can be quantified, providing a measure of enzyme activity. DNPYR-GLYCINE is also utilized in the study of protein structure and function, and its properties make it a valuable tool in various biotechnological and pharmaceutical applications.

3264-08-2

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3264-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3264-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,6 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3264-08:
(6*3)+(5*2)+(4*6)+(3*4)+(2*0)+(1*8)=72
72 % 10 = 2
So 3264-08-2 is a valid CAS Registry Number.

3264-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3,5-dinitro-pyridin-2-yl)-glycine

1.2 Other means of identification

Product number -
Other names (3,5-Dinitro-pyridin-2-ylamino)-acetic acid

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:3264-08-2 SDS

3264-08-2Downstream Products

3264-08-2Relevant academic research and scientific papers

THE REACTIVITY OF SOME PRIMARY AMINES IN SN2Ar REACTIONS WITH 2-CHLORO-3,5-DINITROPYRIDINE

Brenelli, Eugenia Cristina Souza,Moran, Paulo Jose Samenho

, p. 2816 - 2825 (2007/10/02)

Rate constants for SN2Ar reactions of 2-chloro-3,5-dinitropyridine (1) with butylamine, glycine, glycylglycine and ethylenediamine monohydrochloride, in water at 1.0 mol dm-3 constant ionic strength and 25 deg C, have been determined.The Broensted β coefficient is 0.51.The reactivities of 1 and 2-chloro-1-methylpyridinium ion (2) with these primary amines were compared using a derived Edwards equation.One could infer that 2 tends to undergo more charge interaction than 1 because of the quaternary nitrogen of the pyridinium ring of 2.A coordination of the substrates, 1, 2 and 4-chloro-1-methylpyridinium ion (3) dependent on the degree of hardness and softness is presented.

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