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5-Pyrimidinecarbonitrile, 1,2-dihydro-2-oxo(7CI,9CI) is a chemical compound that belongs to the group of pyrimidines, which are heterocyclic aromatic organic compounds. It is a derivative of pyrimidines and is often used in research and scientific studies. 5-Pyrimidinecarbonitrile, 1,2-dihydro-2-oxo(7CI,9CI) is known for its potential applications in various chemical reactions as a chemical intermediate. However, it should be handled with care due to its potential for skin and eye irritation, and damaging effects if inhaled or consumed.

1753-49-7

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1753-49-7 Usage

Uses

Used in Research and Scientific Studies:
5-Pyrimidinecarbonitrile, 1,2-dihydro-2-oxo(7CI,9CI) is used as a chemical intermediate for various reactions in research and scientific studies. Its properties, such as appearance, melting point, or boiling point, can vary based on the conditions it is under and how it's created or stored.
Used in Chemical Reactions:
5-Pyrimidinecarbonitrile, 1,2-dihydro-2-oxo(7CI,9CI) is used as a chemical intermediate in the synthesis of various compounds. Its versatility in reactions makes it a valuable component in the development of new chemical entities and pharmaceuticals.
Used in Pharmaceutical Development:
5-Pyrimidinecarbonitrile, 1,2-dihydro-2-oxo(7CI,9CI) is used as a building block in the development of new pharmaceuticals. Its unique structure and reactivity allow for the creation of novel drug candidates with potential therapeutic applications.
Used in Material Science:
5-Pyrimidinecarbonitrile, 1,2-dihydro-2-oxo(7CI,9CI) is used in the development of new materials with specific properties. Its incorporation into various compounds can lead to the creation of materials with unique characteristics, such as improved stability or enhanced reactivity.
Used in Environmental Applications:
5-Pyrimidinecarbonitrile, 1,2-dihydro-2-oxo(7CI,9CI) is used in the development of new environmental technologies, such as pollution control or waste management. Its chemical properties can be harnessed to create innovative solutions for environmental challenges.

Check Digit Verification of cas no

The CAS Registry Mumber 1753-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1753-49:
(6*1)+(5*7)+(4*5)+(3*3)+(2*4)+(1*9)=87
87 % 10 = 7
So 1753-49-7 is a valid CAS Registry Number.

1753-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-1H-pyrimidine-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 5-cyanopyrimidin-2-one

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:1753-49-7 SDS

1753-49-7Downstream Products

1753-49-7Relevant articles and documents

Process for preparing substituted pyrimidine derivatives

-

, (2008/06/13)

PCT No. PCT/EP98/00074 Sec. 371 Date Dec. 17, 1999 Sec. 102(e) Date Dec. 17, 1999 PCT Filed Jan. 8, 1998 PCT Pub. No. WO98/30549 PCT Pub. Date Jul. 16, 1998A process for preparing substituted pyrimidine derivatives of the general formula (I): in which a [3-(dimethylamino)-2-azaprop-2-en-1-ylidine]dimethylammonium halide is reacted with a substituted acetamide. The compounds of general formula (I) are important intermediate products for pharmaceutical or agrochemical active substances.

Introduction of Carbon Substituents into Pyrimidines by Grignard Reagents

Rise, Frode,Ongstad, Leif,Gacek, Michel,Undheim, Kjell

, p. 613 - 616 (2007/10/02)

Alkyl- and arylmagnesium halides selectively form 1:1-adducts with the heterocyclic ring in substituted 5-cyanopyrimidines.Dehydrogenation gives the corresponding alkyl or aryl substituted pyrimidine.

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