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1H-Imidazole-4,5-dicarbonitrile, 2-(3-fluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40953-39-7

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40953-39-7 Usage

Derivative of imidazole

The compound is based on the imidazole ring structure, which is a common building block in many biologically active compounds.

Contains two nitrile groups

Nitrile groups (C≡N) are highly polar and can form strong hydrogen bonds, making them useful for creating stable compounds with specific properties.

Contains a fluorophenyl group

The presence of a fluorine atom on the phenyl ring can affect the electronic properties of the molecule and can be used to modify its reactivity and solubility.

Used in the synthesis of pharmaceuticals and agrochemicals

The compound can be used as a building block for creating a variety of biologically active compounds, including drugs and pesticides.

Potential applications in medicinal chemistry

The compound's properties and reactivity make it a valuable building block for the development of new drugs and other therapeutic agents.

Used as a reagent in organic synthesis

The compound can be used as a reagent to facilitate chemical reactions and create new compounds.

Diverse potential applications in the fields of pharmaceuticals, agrochemicals, and material science

The compound's unique properties and reactivity make it a valuable building block for a variety of applications, including the development of new materials and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 40953-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,5 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40953-39:
(7*4)+(6*0)+(5*9)+(4*5)+(3*3)+(2*3)+(1*9)=117
117 % 10 = 7
So 40953-39-7 is a valid CAS Registry Number.

40953-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-fluorophenyl)-1H-imidazole-4,5-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 2-(3-fluoro-phenyl)-1H-imidazole-4,5-dicarbonitrile

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:40953-39-7 SDS

40953-39-7Upstream product

40953-39-7Relevant academic research and scientific papers

Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution

Potter, Andrew,Oldfield, Victoria,Nunns, Claire,Fromont, Christophe,Ray, Stuart,Northfield, Christopher J.,Bryant, Christopher J.,Scrace, Simon F.,Robinson, David,Matossova, Natalia,Baker, Lisa,Dokurno, Pawel,Surgenor, Allan E.,Davis, Ben,Richardson, Christine M.,Murray, James B.,Moore, Jonathan D.

scheme or table, p. 6483 - 6488 (2010/12/18)

Pin1 is an emerging oncology target strongly implicated in Ras and ErbB2-mediated tumourigenesis. Pin1 isomerizes bonds linking phospho-serine/threonine moieties to proline enabling it to play a key role in proline-directed kinase signalling. Here we report a novel series of Pin1 inhibitors based on a phenyl imidazole acid core that contains sub-μM inhibitors. Compounds have been identified that block prostate cancer cell growth under conditions where Pin1 is essential.

Imidazoles and their compositions for plant growth regulation

-

, (2008/06/13)

The invention provides a method of regulating the growth of a plant using a compound of the formula: wherein R1 represents alkyl or phenyl optionally substituted by halogen, alkyl, alkoxy, alkylthio, trifluoromethyl, trifluoromethoxy, trifluoromethylthio,

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