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1618-36-6

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1618-36-6 Usage

General Description

4-Chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine is a chemical compound with the molecular formula C7H6N3Cl. It is a heterocyclic compound that contains both nitrogen and chlorine atoms. 4-Chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine has potential applications in the pharmaceutical industry and as a precursor in organic synthesis. It has been studied for its potential uses in medicinal chemistry and drug discovery, with research focusing on its biological activity and potential therapeutic applications. The compound's unique structure and properties make it a promising candidate for future research and development in the field of organic chemistry and drug design.

Check Digit Verification of cas no

The CAS Registry Mumber 1618-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1618-36:
(6*1)+(5*6)+(4*1)+(3*8)+(2*3)+(1*6)=76
76 % 10 = 6
So 1618-36-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClN3/c1-4-2-9-7-5(4)6(8)10-3-11-7/h2-3H,1H3,(H,9,10,11)

1618-36-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine

1.2 Other means of identification

Product number -
Other names 4-chloro-7-methyl-7-deazapurine

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:1618-36-6 SDS

1618-36-6Downstream Products

1618-36-6Relevant articles and documents

Tetrahydropyrrolopyrazoles derivatives Preparation method and application thereof in medicine

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Paragraph 0342-0348, (2021/09/29)

The invention relates to tetrahydropyrrolopyrazol derivatives, a preparation method and an application thereof in medicine. , The present disclosure relates to a tetrahydropyrrolopyrazol derivative represented by the general formula (I), a preparation method thereof, and a use of the derivative-containing pharmaceutical composition and as a therapeutic agent, in particular as AKT1 T1 T1 T1 AKT pan T1 inhibitors and use thereof in the preparation of a medicament for the treatment and/or prevention of tumors.

ASK1 INHIBITING PYRROLOPYRIMIDINE AND PYRROLOPYRIDINE DERIVATIVES

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Paragraph 0154, (2019/02/02)

The present invention relates to pyrrolopyrimidine compounds according to Formula (I) and their use in the prophylaxis and/or treatment of pain, inflammatory conditions, cardiovascular diseases, neurodegenerative diseases, neurological diseases, complications of type I diabetes, cancer and/or fibrotic diseases. In a particular aspect, the present compounds are ASK inhibitors, particularly ASK1 inhibitors. The present invention also provides methods for the production of a compound of the invention, pharmaceutical compositions comprising a compound of the invention, the use of the compounds in the prophylaxis and/or treatment of pain, inflammatory conditions, cardiovascular diseases, neurodegenerative diseases, neurological diseases, complications of type I diabetes, cancer and/or fibrotic diseases. (Formula (I))

Discovery of a 4-aryloxy-1H-pyrrolo[3,2-c]pyridine and a 1-aryloxyisoquinoline series of TRPA1 antagonists

Hu, Yun-Jin,St.-Onge, Miguel,Laliberté, Sébastien,Vallée, Frédéric,Jin, Shujuan,Bedard, Leanne,Labrecque, Jean,Albert, Jeffrey S.

supporting information, p. 3199 - 3203 (2015/02/19)

A series of TRPA1 antagonists is described having a 4-aryloxy-1H-pyrrolo[3,2-c]pyridine or a 1-aryloxyisoquinoline scaffold. These compounds have high ligand efficiency and favorable physical properties and may thus serve as scaffolds for further optimization.

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