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4-Pyrimidin-2-ylbenzoyl chloride is a chemical compound with the molecular formula C13H8ClN3O. It is a benzoyl chloride derivative with a pyrimidine ring attached to the benzene ring. This unique chemical structure makes it valuable in the development of new drugs and materials, and it is used in research and development in the pharmaceutical and chemical industries.

679806-84-9

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679806-84-9 Usage

Uses

Used in Pharmaceutical Industry:
4-Pyrimidin-2-ylbenzoyl chloride is used as a key intermediate in the synthesis of pharmaceuticals for its ability to introduce the benzoyl group into various compounds, contributing to the development of new drugs.
Used in Agrochemical Industry:
4-Pyrimidin-2-ylbenzoyl chloride is used as a key intermediate in the synthesis of agrochemicals, playing a role in the creation of new pesticides or other agricultural products.
Used in Organic Synthesis:
4-Pyrimidin-2-ylbenzoyl chloride is used as a reagent in organic synthesis to introduce the benzoyl group into various compounds, facilitating the formation of new chemical entities for research and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 679806-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,9,8,0 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 679806-84:
(8*6)+(7*7)+(6*9)+(5*8)+(4*0)+(3*6)+(2*8)+(1*4)=229
229 % 10 = 9
So 679806-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H7ClN2O/c12-10(15)8-2-4-9(5-3-8)11-13-6-1-7-14-11/h1-7H

679806-84-9SDS

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 4-pyrimidin-2-ylbenzoyl chloride

1.2 Other means of identification

Product number -
Other names 4-pyrimidin-2-yl-benzoyl chloride

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:679806-84-9 SDS

679806-84-9Relevant academic research and scientific papers

C-H and N-H Bond Annulation of Benzamides with Isonitriles Catalyzed by Cobalt(III)

Kalsi, Deepti,Barsu, Nagaraju,Dahiya, Pardeep,Sundararaju, Basker

supporting information, p. 3937 - 3944 (2017/08/29)

A simple efficient, atom-economical procedure was developed for the cobalt-catalyzed C-H bond annulation of benzamides with isonitriles under mild conditions. The reaction tolerates a variety of functional group including heterocycles. Diverse 3-(alkylimino)-2-quinolin-8-yl-2,3-dihydro-1 H -isoindol-1-ones were synthesized using isonitriles as the C1 source through C-H and N-H bond annulation via C-H bond activation in a 'green' solvent. Vinylamides were also used similarly with tert -butyl isonitrile to give 3-(tert -butylimino)-1-quinolin-8-yl-1 H -pyrrol-2(5 H)-ones.

Pyrrolobenzodiazepine pyridine carboxamides and derivatives as follicle-stimulating hormone receptor antagonists

-

Page/Page column 51, (2010/11/25)

This invention provides pyrrolobenzodiazepine pyridine carboxamides selected from those of Formula (1), which act as follicle stimulating hormone receptor antagonists. The invention also provides pharmaceutical compositions and methods of treatment utilizing the compounds of Formulae (1) and (2).

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