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2-chloro-4-methyl-6-phenylpyrimidine is a chemical compound with the molecular formula C11H9ClN2. It is a white to off-white crystalline solid and is classified as an organochlorine compound.

32785-40-3

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32785-40-3 Usage

Uses

Used in Pharmaceutical Industry:
2-chloro-4-methyl-6-phenylpyrimidine is used as an intermediate in the production of pharmaceuticals for its potential role in the synthesis of various drug molecules.
Used in Agrochemical Industry:
2-chloro-4-methyl-6-phenylpyrimidine is used as an intermediate in the production of agrochemicals, contributing to the development of pesticides and other agricultural chemicals.
Used in Organic Synthesis:
2-chloro-4-methyl-6-phenylpyrimidine serves as a building block in organic synthesis, enabling the creation of a range of organic compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 32785-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,8 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32785-40:
(7*3)+(6*2)+(5*7)+(4*8)+(3*5)+(2*4)+(1*0)=123
123 % 10 = 3
So 32785-40-3 is a valid CAS Registry Number.

32785-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-4-methyl-6-phenylpyrimidine

1.2 Other means of identification

Product number -
Other names 2-chloro-4-phenyl-6-methylpyrimidine

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:32785-40-3 SDS

32785-40-3Relevant academic research and scientific papers

N^N^C platinum (II) complexes based on phenyl-pyridin-2-ylpyrimidine ligands: synthesis, electrochemical and photophysical properties

Achelle, Sylvain,Boixel, Julien,Gauthier, Sébastien,Guen, Fran?oise Robin-le,Hruzd, Mariia,Kahlal, Samia,Saillard, Jean-Yves,le Poul, Nicolas

, (2021/07/13)

A series of luminescent chloro- and alkynyl-platinum (II) complexes containing various tridentate cyclometalated ligands derived from phenyl-pyridin-2-ylpyrimidine and alkynyl ligands has been successfully synthesized and characterized. Their electrochemical, electronic absorption and luminescence properties have been experimentally investigated and supported by (Time-Dependent) Density Functional Theory ((TD)-DFT) calculations. Electrochemical studies show the presence of a ligand-centered reduction originating from the cyclometalating N^N^C ligands, as well as a major ligand-centered oxidation process (N^N^C or alkynyl) with minor contributions of the metal. Most of the complexes exhibits yellow-to-red luminescence at room-temperature in diluted solutions, in frozen matrices and in the solid state. Electron-withdrawing groups on the alkynyl-ligand induce a red shift of the emission band with increased quantum yield in solution. The emission is also sensitive to the position of the pyridyl fragment on the pyrimidine core: complexes with electron-poorer 4-pyridin-2-ylpyrimidine ligands exhibit red-shifted emission and decreased quantum yield compared to their 2-pyridin-4yl analogues. In solid state, chloro-platinum complexes without tBu bulky group exhibit red-shifted excimer emission.

Discovery of 2-(cyclohexylmethylamino)pyrimidines as a new class of reversible valosine containing protein inhibitors

Cervi, Giovanni,Magnaghi, Paola,Asa, Daniela,Avanzi, Nilla,Badari, Alessandra,Borghi, Daniela,Caruso, Michele,Cirla, Alessandra,Cozzi, Liviana,Felder, Eduard,Galvani, Arturo,Gasparri, Fabio,Lomolino, Antonio,Magnuson, Steven,Malgesini, Beatrice,Motto, Ilaria,Pasi, Maurizio,Rizzi, Simona,Salom, Barbara,Sorrentino, Graziella,Troiani, Sonia,Valsasina, Barbara,O'Brien, Thomas,Isacchi, Antonella,Donati, Daniele,D'Alessio, Roberto

, p. 10443 - 10454 (2015/02/19)

Valosine-containing protein (VCP), also known as p97 or cdc48 in yeast, is a highly abundant protein belonging to the AAA ATPase family involved in a number of essential cellular functions, including ubiquitin-proteasome mediated protein degradation, Golgi reassembly, transcription activation, and cell cycle control. Altered expression of VCP has been detected in many cancer types sometimes associated with poor prognosis. Furthermore, VCP mutations are causative of some neurodegenerative disorders. In this paper we report the discovery, synthesis, and structure-activity relationships of substituted 2-aminopyrimidines, representing a new class of reversible VCP inhibitors. This class of compounds, identified in a HTS campaign against recombinant VCP, has been progressively expanded and manipulated to increase biochemical potency and gain cellular activity.

NOVEL PYRROLIDINE DERIVED BETA 3 ADRENERGIC RECEPTOR AGONISTS

-

Page/Page column 47, (2011/04/14)

The present invention provides compounds of Formula (I), pharmaceutical compositions thereof, and method of using the same in the treatment or prevention of diseases mediated by the activation of β3-adrenoceptor.

Nickel-catalyzed Addition or Coupling Reactions of Grignard Reagents with Halopyrimidines

Elmoghayar, Mohamed R. H.,Groth, Per,Undheim, Kjell

, p. 109 - 114 (2007/10/02)

Phenylmagnesium bromide with NiCl2(dppp) catalysis adds selectively to the unsubstituted position in 2,4-dichlro-5-chloro(fluoro)pyrimidine.X-Ray structure analysis of the hydrolyzed adduct shows an infinite chain by N1 - N3' hydrogen bonding.The hydrolyz

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