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2-AMINO-4-CHLORO-6-OXO-1,6-DIHYDROPYRIMIDINE-5-CARBONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85840-23-9

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85840-23-9 Usage

Chemical compound

2-AMINO-4-CHLORO-6-OXO-1,6-DIHYDROPYRIMIDINE-5-CARBONITRILE

Class

Dihydropyrimidines

Substituents

Amino group, chlorine atom, cyano group

Ring structure

Six-membered dihydropyrimidine

Properties

Antiviral, antitumor, antituberculosis

Applications

Pharmaceutical and agrochemical industries

Use

Intermediate in synthesis of pharmaceutical compounds, building block in production of complex organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 85840-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,4 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85840-23:
(7*8)+(6*5)+(5*8)+(4*4)+(3*0)+(2*2)+(1*3)=149
149 % 10 = 9
So 85840-23-9 is a valid CAS Registry Number.

85840-23-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-chloro-4-oxo-1H-pyrimidine-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Amino-4-chloro-6-oxo-1,6-dihydropyrimidine-5-carbonitrile

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:85840-23-9 SDS

85840-23-9Relevant academic research and scientific papers

Adenosine receptor ligands and their use in the treatment of disease

-

, (2008/06/13)

The invention relates to cyclic heteroaromatic compounds, containing at least one nitrogen atom, and to their use in the manufacture of medicaments for the treatment of diseases, related to adenosine receptor modulators, such as Alzheimer's disease, Parkinson's disease, neuroprotection, schizophrenia, anxiety, pain, respiration deficits, depression, asthma, allergic responses, hypoxia, ischaemia, seizure, substance abuse, sedation and they may be active as muscle relaxants, antipsychotics, anti epileptics, anticonvulsants and cardiaprotective agents.

Chemistry of 5-Pyrimidinecarboxaldehydes

Bell, Lawrence,McGuire, H. Michael,Freeman, G. Andrew

, p. 41 - 44 (2007/10/02)

Selective hydrolysis of 2-amino-4,6-dichloro-5-pyrimidinecarboxaldehyde, 2, gave 2-amino-4-chloro-1,6-dihydro-6-oxo-5-pyrimidinecarboxaldehyde, 5.The oxime of 2 rearranged to 2-amino-4-chloro-1,6-dihydro-6-oxo-5-pyrimidinecarbonitrile, 8.Reaction of 8 wit

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