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66131-68-8

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66131-68-8 Usage

General Description

4-Pyrimidinamine, 2-chloro-N-methyl- (9CI) is a chemical compound with the molecular formula C5H6ClN3. It is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. 4-Pyrimidinamine, 2-chloro-N-methyl- (9CI) is a derivative of pyrimidinamine, a heterocyclic organic compound, with a chlorine atom and a methyl group attached to the nitrogen atom. It is known for its unique chemical properties and is utilized in various research and industrial applications. Its structural features make it suitable for use in the development of new drugs and chemical compounds. Additionally, it plays a crucial role in the advancement of organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 66131-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,3 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66131-68:
(7*6)+(6*6)+(5*1)+(4*3)+(3*1)+(2*6)+(1*8)=118
118 % 10 = 8
So 66131-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H6ClN3/c1-7-4-2-3-8-5(6)9-4/h2-3H,1H3,(H,7,8,9)

66131-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-methylpyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names 2-chloro-N-methyl-4-pyrimidinamine

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:66131-68-8 SDS

66131-68-8Relevant articles and documents

Selectivity, ligand deconstruction, and cellular activity analysis of a BPTF bromodomain inhibitor

Kirberger, Steven E.,Ycas, Peter D.,Johnson, Jorden A.,Chen, Chen,Ciccone, Michael F.,Woo, Rinette W. L.,Urick, Andrew K.,Zahid, Huda,Shi, Ke,Aihara, Hideki,McAllister, Sean D.,Kashani-Sabet, Mohammed,Shi, Junwei,Dickson, Alex,Dos Santos, Camila O.,Pomerantz, William C. K.

supporting information, p. 2020 - 2027 (2019/02/20)

Bromodomain and PHD finger containing protein transcription factor (BPTF) is an epigenetic protein involved in chromatin remodelling and is a potential anticancer target. The BPTF bromodomain has one reported small molecule inhibitor (AU1, rac-1). Here, advances made on the structure-activity relationship of a BPTF bromodomain ligand are reported using a combination of experimental and molecular dynamics simulations leading to the active enatiomer (S)-1. Additionally, a ligand deconstruction analysis was conducted to characterize important pharmacophores for engaging the BPTF bromodomain. These studies have been enabled by a protein-based fluorine NMR approach, highlighting the versatility of the method for selectivity, ligand deconstruction, and ligand binding. To enable future analysis of biological activity, cell growth analyses in a panel of cancer cell lines were carried out using CRISPR-Cas9 and (S)-1 to identify cell-based model systems that are sensitive to BPTF inhibition.

USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS

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Paragraph 00412-00413, (2016/04/20)

The present disclosure provides methods of treating and/or preventing inflammatory bowel disease (IBD) and graft-versus-host disease (GVHD) using salt-inducible kinase (SIK) inhibitors, such as macrocyclic SIK inhibitors of Formula (I), imidazolyl SIK inh

2-PHENYLAMINOPYRIMIDINE DERIVATIVES AS KINASE LRRK2 MODULATORS FOR THE TREATMENT OF PARKINSON'S DISEASE

-

Page/Page column 57, (2013/06/27)

Specific Compounds of formula (I): or pharmaceutically acceptable salts thereof, wherein m, X, R, R2, R3, R, R6 and R7 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with LRRK2 receptor, such as Parkinson's disease.

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