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2-Pyrimidinamine, 4-(5-methyl-3-phenyl-4-isoxazolyl)-, also known as 4-(5-methyl-3-phenyl-4-isoxazolyl)pyrimidin-2-amine, is a chemical compound with the molecular formula C13H11N3O and a molecular weight of 225.24 g/mol. It is a derivative of pyrimidinamine, featuring a 5-methyl-3-phenyl-4-isoxazolyl group attached to the 4-position of the pyrimidine ring. 2-Pyrimidinamine, 4-(5-methyl-3-phenyl-4-isoxazolyl)- is of interest in the field of organic chemistry and may have potential applications in the development of pharmaceuticals or other chemical products. Its structure and properties make it a valuable building block for the synthesis of more complex molecules.

264256-23-7

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264256-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 264256-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,4,2,5 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 264256-23:
(8*2)+(7*6)+(6*4)+(5*2)+(4*5)+(3*6)+(2*2)+(1*3)=137
137 % 10 = 7
So 264256-23-7 is a valid CAS Registry Number.

264256-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)pyrimidin-2-amine

1.2 Other means of identification

Product number -
Other names 4-(5-methyl-3-phenylisoxazol-4-yl)pyrimidin-2-ylamine

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 -
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More Details:264256-23-7 SDS

264256-23-7Relevant academic research and scientific papers

Inhibitors of c-Jun N terminal kinases (JNK) and other protein kinases

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, (2008/06/13)

The present invention provides compounds of formula I: 1where R1 is H, CONH2, T(n)—R, or T(n)—Ar2, n may be zero or one, and G, XYZ, and Q are as described below. These compounds are inhibitors of protein kinase, particularly inhibitors of JNK, a mammalian protein kinase involved cell proliferation, cell death and response to extracellular stimuli. The invention also relates to methods for producing these inhibitors. The invention also provides pharmaceutical compositions comprising the inhibitors of the invention and methods of utilizing those compositions in the treatment and prevention of various disorders.

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