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34253-01-5

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34253-01-5 Usage

General Description

Methyl pyrimidine-5-carboxylate is a chemical compound with the molecular formula C7H7NO2. It is a derivative of pyrimidine with a methyl group and carboxylate functional groups attached to the fifth carbon atom. Methyl pyrimidine-5-carboxylate is commonly used in the synthesis of pharmaceuticals and agrochemicals due to its role as a building block in organic chemistry. It is also studied for its potential biological and pharmacological activities. Methyl pyrimidine-5-carboxylate can be synthesized through various chemical reactions and is commercially available for research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 34253-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,5 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34253-01:
(7*3)+(6*4)+(5*2)+(4*5)+(3*3)+(2*0)+(1*1)=85
85 % 10 = 5
So 34253-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c1-10-6(9)5-2-7-4-8-3-5/h2-4H,1H3

34253-01-5 Well-known Company Product Price

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  • Aldrich

  • (682241)  Methylpyrimidine-5-carboxylate  95%

  • 34253-01-5

  • 682241-1G

  • 1,573.65CNY

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34253-01-5SDS

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 METHYL PYRIMIDINE-5-CARBOXYLATE

1.2 Other means of identification

Product number -
Other names Pyrimidin-5-carbonsaeure-methylester

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:34253-01-5 SDS

34253-01-5Relevant articles and documents

METHODS AND COMPOUNDS FOR INHIBITING MRP1

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, (2008/06/13)

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Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents

Young, Jonathan R.,Huang, Song X.,Chen, Irene,Walsh, Thomas F.,DeVita, Robert J.,Wyvratt Jr., Matthew J.,Goulet, Mark T.,Ren, Ning,Lo, Jane,Yang, Yi Tien,Yudkovitz, Joel B.,Cheng, Kang,Smith, Roy G.

, p. 1723 - 1727 (2007/10/03)

A series of 3-arylquinolones was prepared and evaluated for their ability to act as gonadotropin releasing hormone (GnRH) antagonists. A variety of substitution patterns of the 3-aryl substituent are described. The 3,4,5-trimethylphenyl substituent (23h) was found to be optimal. (C) 2000 Elsevier Science Ltd. All rights reserved.

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