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31058-83-0

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31058-83-0 Usage

General Description

"(6-Chloro-pyrimidin-4-yl)-dimethyl-amine" is a chemical compound that belongs to the class of organic compounds known as aminopyrimidines and derivatives. This specific compound features a pyrimidine ring, which is a six-member ring with two nitrogen atoms and four carbon atoms, further substituted by a chlorine atom and two methyl groups attached through a nitrogen atom. The detailed information about this compound, such as its physical and chemical properties or its potential uses, is not commonly found in public sources, suggesting it may not be widely used or extensively studied. Detailed investigations may be needed to understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 31058-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,5 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31058-83:
(7*3)+(6*1)+(5*0)+(4*5)+(3*8)+(2*8)+(1*3)=90
90 % 10 = 0
So 31058-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H8ClN3/c1-10(2)6-3-5(7)8-4-9-6/h3-4H,1-2H3

31058-83-0 Well-known Company Product Price

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  • Aldrich

  • (CBR00409)  6-Chloro-N,N-dimethylpyrimidin-4-amine  AldrichCPR

  • 31058-83-0

  • CBR00409-1G

  • 2,255.76CNY

  • Detail

31058-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-N,N-dimethylpyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names 6-Chloro-N,N-dimethylpyrimidin-4-amine

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:31058-83-0 SDS

31058-83-0Relevant articles and documents

Discovery of BAY-985, a Highly Selective TBK1/IKK? Inhibitor

Lefranc, Julien,Schulze, Volker Klaus,Hillig, Roman Christian,Briem, Hans,Prinz, Florian,Mengel, Anne,Heinrich, Tobias,Balint, Jozsef,Rengachari, Srinivasan,Irlbacher, Horst,St?ckigt, Detlef,B?mer, Ulf,Bader, Benjamin,Gradl, Stefan Nikolaus,Nising, Carl Friedrich,Von Nussbaum, Franz,Mumberg, Dominik,Panne, Daniel,Wengner, Antje Margret

, p. 601 - 612 (2020/02/04)

The serine/threonine kinase TBK1 (TANK-binding kinase 1) and its homologue IKK? are noncanonical members of the inhibitor of the nuclear factor κB (IκB) kinase family. These kinases play important roles in multiple cellular pathways and, in particular, in inflammation. Herein, we describe our investigations on a family of benzimidazoles and the identification of the potent and highly selective TBK1/IKK? inhibitor BAY-985. BAY-985 inhibits the cellular phosphorylation of interferon regulatory factor 3 and displays antiproliferative efficacy in the melanoma cell line SK-MEL-2 but showed only weak antitumor activity in the SK-MEL-2 human melanoma xenograft model.

Regioselective metalations of pyrimidines and pyrazines by using frustrated Lewis pairs of BF3×OEt2 and hindered magnesium- and zinc-amide bases

Groll, Klaus,Manolikakes, Sophia M.,Du Jourdin, Xavier Mollat,Jaric, Milica,Bredihhin, Aleksei,Karaghiosoff, Konstantin,Carell, Thomas,Knochel, Paul

supporting information, p. 6776 - 6780 (2013/07/26)

Born of frustration: Using the frustrated Lewis pairs TMP-metal and BF 3×OEt2 allows the regioselective metalation of pharmaceutically relevant diazines, such as pyrimidines, purines, and pyrazines. These metalations are often complementary to prior deprotonations performed without BF3×OEt2. Especially attractive is a new sequential regioselective full functionalization of the pyrazine scaffold with a bulky (TMS)2CH substituent. Copyright

PYRIMIDINE DERIVATIVES AND METHODS OF TREATMENT RELATED TO THE USE THEREOF

-

Page/Page column 106, (2008/06/13)

The present invention encompasses novel substituted pyrimidine compounds of Formula (I): which act as MCH receptor antagonists. These compounds are useful in pharmaceutical compositions whose use includes prophylaxis or treatment of improving memory function, sleeping and arousal, anxiety, depression, mood disorders, seizure, obesity, diabetes, appetite and eating disorders, cardiovascular disease, hypertension, dyslipidemia, myocardial infarction, binge eating disorders including bulimia, anorexia, mental disorders including manic depression, schizophrenia, delirium, dementia, stress, cognitive disorders, attention deficit disorder, substance abuse disorders and dyskinesias including Parkinson’s disease, epilepsy, and addiction.

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