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7084-55-1

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7084-55-1 Usage

General Description

2,6-diamino-5-[(4-nitrophenyl)hydrazono]pyrimidin-4(5H)-one is a chemical compound with the molecular formula C10H9N7O3. It is a pyrimidine derivative with two amino groups and a hydrazono group attached to a nitrophenyl moiety. 2,6-diamino-5-[(4-nitrophenyl)hydrazono]pyrimidin-4(5H)-one has potential applications in pharmaceuticals and agrochemicals due to its ability to act as a building block for the synthesis of various biologically active molecules. Additionally, it has been studied for its anti-inflammatory and anti-cancer properties. However, further research is needed to fully understand its potential uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 7084-55-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7084-55:
(6*7)+(5*0)+(4*8)+(3*4)+(2*5)+(1*5)=101
101 % 10 = 1
So 7084-55-1 is a valid CAS Registry Number.

7084-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5E)-2,6-diamino-5-[(4-nitrophenyl)hydrazinylidene]pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 5-(4'-Nitrophenylazo)-2,4-diamino-6-hydroxy-pyrimidin

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:7084-55-1 SDS

7084-55-1Downstream Products

7084-55-1Relevant articles and documents

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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