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924644-04-2

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924644-04-2 Usage

Explanation

The compound is composed of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms, with 16 carbon atoms, 14 hydrogen atoms, 4 nitrogen atoms, and 2 oxygen atoms.

Explanation

The total mass of one mole of the compound, calculated by adding the atomic weights of all the atoms in the molecular formula.

Explanation

The compound is formed by attaching a phenylmethyl group (a benzene ring with a methyl group) to a piperazinecarboxylic acid molecule, with additional 4-(4-amino-2-pyrimidinyl) substituents.

Explanation

The compound has been studied for its potential use in treating diseases such as cancer and infectious diseases, making it a promising candidate for further research and development.

Explanation

The compound's chemical structure and properties make it a possible candidate for antiviral and antitumor therapies, which could lead to new treatments for these conditions.

Explanation

The compound is an organic molecule with a complex structure, containing multiple functional groups and a large number of atoms.

Molecular weight

302.32 g/mol

Chemical structure

A phenylmethyl ester derivative of piperazinecarboxylic acid with 4-(4-amino-2-pyrimidinyl) substituents.

Usage in pharmaceutical industry

Potential treatment for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 924644-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,6,4 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 924644-04:
(8*9)+(7*2)+(6*4)+(5*6)+(4*4)+(3*4)+(2*0)+(1*4)=172
172 % 10 = 2
So 924644-04-2 is a valid CAS Registry Number.

924644-04-2Downstream Products

924644-04-2Relevant articles and documents

Inhibitors of P2X3

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Page/Page column 10, (2008/06/13)

Compounds of formula 1 are modulators of P2X3 useful for the treatment of pain and genito-urinary, gastrointestinal, and respiratory disorders: wherein R1 is —C(═S)CH3, pyridyl, pyrimidinyl, pyrazinyl, thiazolyl, furyl, furylcarbonyl, acetyl, or carbamoyl; R2a and R2b are independently H, methyl, or ethyl; R3 is H or methyl; Y is a bond, —(CR4R5)n— or —CR4═CR5—; wherein R4 and R5 are each independently H or methyl and n is 1 or 2; X is N or CH; A is phenyl, 5-membered heterocyclyl, or 6-membered heterocyclyl; R6, R7 and R8 are each independently H, halo, lower alkyl, cycloalkyl, alkylthio, alkylthio-lower alkyl, alkylsulfonyl-lower alkyl, di(lower alkyl)amino-lower alkyl, morpholinyl-lower alkyl, 4-methyl-piperazinyl-methyl, trifluoromethyl, pyridyl, tetrazolyl, thiophenyl, phenyl, biphenyl, or benzyl (where thiophenyl, phenyl and benzyl are substituted with 0-3 lower alkyl, halo, sulfonamido, trifluoromethyl, lower alkoxy or lower alkylthio) or R6 and R7 together form a 5-membered or 6-membered carbocyclic or heterocyclic ring substituted with 0-3 substituents selected from the group consisting of lower alkyl, lower alkoxy, oxo, halo, thiophenyl-lower alkyl, phenyl, benzyl (where phenyl and benzyl are substituted with 0-3 lower alkyl, halo, sulfonamido, trifluoro-methyl, lower alkoxy, lower alkylthio, amino-lower alkyl, lower alkylamino-lower alkyl, or di(lower alkyl)amino-lower alkyl); and pharmaceutically acceptable salts thereof; wherein when R1 is pyrimidin-2-yl, X is N, Y is a bond and A is oxazol-5-yl the carbon atom at position 4 in said oxazol-5-yl is not substituted by propyl when the carbon atom at position 2 in said oxazol-5-yl is substituted by substituted phenyl and the carbon atom at position 4 in said oxazol-5-yl is not substituted by phenyl when the carbon atom at position 2 is substituted by unsubstituted or substituted phenyl.

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