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23899-73-2

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23899-73-2 Usage

Structure

Heterocyclic compound with a pyrimidine ring structure and two amino groups at positions 4 and 5

Applications

Potential use in the pharmaceutical industry for the development of antiviral and anticancer drugs, can also be used as a building block for the synthesis of other organic compounds

Biological activities

Has been studied for its potential therapeutic uses and biological activities

Check Digit Verification of cas no

The CAS Registry Mumber 23899-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,9 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23899-73:
(7*2)+(6*3)+(5*8)+(4*9)+(3*9)+(2*7)+(1*3)=152
152 % 10 = 2
So 23899-73-2 is a valid CAS Registry Number.

23899-73-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-diaminopyrimidin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 4,5-Diamino-1H-pyrimidin-2-on

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:23899-73-2 SDS

23899-73-2Relevant articles and documents

Phenyl-imidazolo-cytidine analogues: Structure-photophysical activity relationship and ability to detect single dna mismatch

Kovaliov, Marina,Weitman, Michal,Major, Dan Thomas,Fischer, Bilha

, p. 7051 - 7062 (2014/08/18)

To expand the arsenal of fluorescent cytidine analogues for the detection of genetic material, we synthesized para-substituted phenyl-imidazolo-cytidine (PhImC) analogues 5a-g and established a relationship between their structure and fluoresce

3-deoxyglucosone and skin

-

, (2008/06/13)

The invention relates to a method of removing 3-deoxyglucosone and other alpha-dicarbonyl sugars from skin. The invention further relates to methods of inhibiting production and function of 3-deoxyglucosone and other alpha-dicarbonyl sugars in skin. The invention also relates to methods of treating 3-deoxyglucosone and other alpha-dicarbonyl sugars associated diseases and disorders of skin.

Amino-substituted pyrimidines, derivatives and methods of use therefor

-

, (2008/06/13)

The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging). Accordingly, a composition is disclosed which comprises an agent capable of inhibiting the formation of advanced glycosylation end products of target proteins by reacting with the carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation. The method comprises contacting the target protein with the composition. Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.

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