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7501-32-8

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7501-32-8 Usage

General Description

N-(4-Amino-6-chloropyrimidin-5-yl)formamide is a chemical compound that belongs to the class of amides. It has a molecular formula C5H6ClN5O and a molecular weight of 175.59 g/mol. N-(4-AMino-6-chloropyriMidin-5-yl)forMaMide is a derivative of pyrimidine, a heterocyclic organic compound that is commonly found in nucleic acids such as DNA and RNA. N-(4-Amino-6-chloropyrimidin-5-yl)formamide is used in the synthesis of pharmaceuticals and agrochemicals, and it has potential applications in the field of medicinal chemistry. It is a valuable building block in organic synthesis and has the potential to be used in the development of new drug compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 7501-32-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7501-32:
(6*7)+(5*5)+(4*0)+(3*1)+(2*3)+(1*2)=78
78 % 10 = 8
So 7501-32-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H5ClN4O/c6-4-3(10-2-11)5(7)9-1-8-4/h1-2H,(H,10,11)(H2,7,8,9)

7501-32-8SDS

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 N-(4-amino-6-chloropyrimidin-5-yl)formamide

1.2 Other means of identification

Product number -
Other names 4-amino-6-chloro-5-formamido-pyrimidine

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:7501-32-8 SDS

7501-32-8Downstream Products

7501-32-8Relevant articles and documents

Nitrosopurines en route to potently cytotoxic asmarines

Wan, Kanny K.,Iwasaki, Kotaro,Umotoy, Jeffrey C.,Wolan, Dennis W.,Shenvi, Ryan A.

, p. 2410 - 2415 (2015/03/04)

A nitrosopurine ene reaction easily assembles the asmarine pharmacophore and transmits remote stereochemistry to the diazepine-purine hetereocycle. This reaction generates potent cytotoxins which exceed the potency of asmarine A (1.2 μM IC50) and supersede the metabolites as useful leads for biological discovery.

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