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A pyrimidine derivative with two amino groups and a phenylmethylideneamino substituent

25477-74-1

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25477-74-1 Usage

Biological activities

Potential biological activities

Uses

Building block in organic synthesis and pharmaceutical applications

Potential applications

Development of new drugs for various medical conditions

Versatile compound

Suitable for further research and potential applications in medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 25477-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,7 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25477-74:
(7*2)+(6*5)+(5*4)+(4*7)+(3*7)+(2*7)+(1*4)=131
131 % 10 = 1
So 25477-74-1 is a valid CAS Registry Number.

25477-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-diamino-5-(benzylideneamino)-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 4(3H)-Pyrimidinone,2,6-diamino-5-benzylidenamino

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:25477-74-1 SDS

25477-74-1Downstream Products

25477-74-1Relevant academic research and scientific papers

Studies on the series of azoles and azines. 66. Synthesis, spectra and structure of 5-arylazo- and 5-arylideneamino-2,4,6-triaminopyrimidines and their 6-hydroxy analogs

Belodedova,Smorygo,Mirzoyan,Melik-Orandzhanyan,Studentsov,Ivin

, p. 538 - 545 (2007/10/02)

5-Arylazo and 5-arylideneamino-2,4,6-triaminopyrimidines and their 6-hydroxy analogs were obtained by azo coupling of 2,4,6-triamino- and 2,4-diamino-6-hydroxypyrimidines with aryldiazonium salts, and also by the reaction of benzaldehydes with 2,4,5,6-tetraamino- and 2,4,5-triamino-6-hydroxypyrimidines, respectively. According to spectral data, in solvents with different polarity, these compounds exist preferentially in the triamino- or diaminohydroxy form. The main paths of the mass spectrometric fragmentation of the compounds studied have been determined.

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