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ETHYL 5-PYRIMIDINECARBOXYLATE 98 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40929-50-8

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40929-50-8 Usage

Synthesis Reference(s)

Synthetic Communications, 24, p. 253, 1994 DOI: 10.1080/00397919408013824Tetrahedron Letters, 25, p. 5939, 1984 DOI: 10.1016/S0040-4039(01)81726-3

Check Digit Verification of cas no

The CAS Registry Mumber 40929-50-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,2 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40929-50:
(7*4)+(6*0)+(5*9)+(4*2)+(3*9)+(2*5)+(1*0)=118
118 % 10 = 8
So 40929-50-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c1-2-11-7(10)6-3-8-5-9-4-6/h3-5H,2H2,1H3

40929-50-8 Well-known Company Product Price

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  • Aldrich

  • (549738)  Ethyl5-pyrimidinecarboxylate  98%

  • 40929-50-8

  • 549738-1G

  • 212.94CNY

  • Detail
  • Aldrich

  • (549738)  Ethyl5-pyrimidinecarboxylate  98%

  • 40929-50-8

  • 549738-5G

  • 639.99CNY

  • Detail

40929-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-Pyrimidinecarboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 5-pyrimidinecarboxylate

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:40929-50-8 SDS

40929-50-8Relevant academic research and scientific papers

MULTISUBSTITUTED AROMATIC COMPOUNDS AS INHIBITORS OF THROMBIN

-

Paragraph 0359-0363, (2017/12/07)

There are provided inter alia multisubstituted aromatic compounds useful for the inhibition of thrombin, which compounds include substituted pyrazolyl or substituted triazolyl. There are additionally provided pharmaceutical compositions. There are additionally provided methods of treating and preventing a disease or disorder, which disease or disorder is amenable to treatment or prevention by the inhibition of thrombin.

MULTISUBSTITUTED AROMATIC COMPOUNDS AS SERINE PROTEASE INHIBITORS

-

Paragraph 0244, (2014/09/29)

There are provided inter alia multisubstituted aromatic compounds useful for the inhibition of kallikrein, which compounds include substituted pyrazolyl or substituted triazolyl. There are additionally provided pharmaceutical compositions. There are additionally provided methods of treating and preventing certain diseases or disorders, which disease or disorder is amenable to treatment or prevention by the inhibition of kallikrein.

MULTISUBSTITUTED AROMATIC COMPOUNDS AS INHIBITORS OF THROMBIN

-

Page/Page column 92, (2011/10/31)

There are provided inter alia multisubstituted aromatic compounds useful for the inhibition of thrombin, which compounds include substituted pyrazolyl or substituted triazolyl. There are additionally provided pharmaceutical compositions. There are additionally provided methods of treating and preventing a disease or disorder, which disease or disorder is amenable to treatment or prevention by the inhibition of thrombin.

One-pot synthesis of pyrimidine-5-carboxaldehyde and ethyl pyrimidine -5- carboxylate by utilizing pyrimidin-5-yl-lithium

Rho,Abuh

, p. 253 - 256 (2007/10/02)

Pyrimidine-5-carboxaldehyde was prepared in a one-pot reaction from 5- bromo-pyrimidine via metal halogen exchange. Pyrimidin-5-yl-lithium reacted with formate ester and ethyl cyanoformate, forming respectively the aldehyde and carboxy ethyl ester.

PALLADIUM CATALYSED SYNTHESIS OF N AND S HETEROCYCLIC ESTERS

Head, Robert A.,Ibbotson, Arthur

, p. 5939 - 5942 (2007/10/02)

Palladium catalysed alkoxycarbonylation of heterocyclic halides affords a simple and versatile synthesis of both N and S heterocyclic esters where a range of catalysts have been studied and a method to employ inexpensive inorganic bases has been found.

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