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1131992-22-7

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1131992-22-7 Usage

General Description

2,4-Dichloro-7-(phenylsulfonyl)-7H-Pyrrolo[2,3-d]pyrimidine is a chemical compound with the molecular formula C15H8Cl2N2O2S. It is a pyrrolopyrimidine derivative that contains two chlorine atoms and a phenylsulfonyl group. 2,4-Dichloro-7-(phenylsulfonyl)-7H-Pyrrolo[2,3-d]pyrimidine has been studied for its potential use as a pharmaceutical agent, particularly in the field of medicinal chemistry. Its structure and properties make it a promising candidate for further research and development as a potential therapeutic agent for various medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1131992-22-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,1,9,9 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1131992-22:
(9*1)+(8*1)+(7*3)+(6*1)+(5*9)+(4*9)+(3*2)+(2*2)+(1*2)=137
137 % 10 = 7
So 1131992-22-7 is a valid CAS Registry Number.

1131992-22-7Relevant articles and documents

Heterocyclic Adenosine Receptor Antagonists

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Paragraph 0320; 0321-0322, (2021/09/26)

Heterocyclic compounds useful as antagonists of adenosine receptors, and methods of treatment of diseases using antagonists of adenosine receptors are disclosed herein. Also disclosed herein are pharmaceutical compositions and methods of administration of

Key intermediate for synthesis of CDK 4/6 dual inhibitor and preparation method and application of key intermediate

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Paragraph 0057-0060; 0088-0091; 0103-0106, (2019/08/20)

The invention discloses a 2-chloro-7-cyclopentyl-N,N-dimethyl-7H-pyrrolo[2,3-d]pyrimidine-6-methanamide intermediate and a preparation method and application thereof. The intermediate is the compoundI, and the preparation method comprises the following st

PYRROLOPYRIMIDINE COMPOUNDS

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Page/Page column 32-33; 15, (2009/04/25)

Compounds of formula (I) are A2B receptor antagonists: wherein Ri is optionally substituted aryl or an optionally substituted monocyclic heteroaryl group having 5 or 6 ring atoms; R2 and R3 are independently selected from

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