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4-NITRO-3-(TRIFLUOROMETHYL)BENZONITRILE&, with the molecular formula C8H3F3N2O2, is a pale yellow crystalline solid that serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals. As a nitrobenzene derivative, it is recognized for its strong electron-withdrawing properties, which are instrumental in various chemical reactions and transformations. The presence of a trifluoromethyl group endows the compound with unique and powerful properties, enhancing its value in medicinal and agricultural research and development.

320-36-5

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320-36-5 Usage

Uses

Used in Pharmaceutical Industry:
4-NITRO-3-(TRIFLUOROMETHYL)BENZONITRILE& is used as a key intermediate in the synthesis of anti-inflammatory drugs, leveraging its electron-withdrawing properties to contribute to the drug's therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 4-NITRO-3-(TRIFLUOROMETHYL)BENZONITRILE& is utilized as a building block for the development of pesticides and herbicides, where its unique properties help in the creation of effective and targeted agrochemicals.
Used in Organic Synthesis:
4-NITRO-3-(TRIFLUOROMETHYL)BENZONITRILE& is employed as a valuable building block in organic synthesis, particularly for the preparation of heterocyclic compounds and biologically active molecules, due to its strong electron-withdrawing nature and the influence of the trifluoromethyl group.

Check Digit Verification of cas no

The CAS Registry Mumber 320-36-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 320-36:
(5*3)+(4*2)+(3*0)+(2*3)+(1*6)=35
35 % 10 = 5
So 320-36-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H3F3N2O2/c9-8(10,11)6-3-5(4-12)1-2-7(6)13(14)15/h1-3H

320-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitro-3-(trifluoromethyl)benzonitrile

1.2 Other means of identification

Product number -
Other names 4-Nitro-3-trifluormethyl-benzonitril

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:320-36-5 SDS

320-36-5Relevant academic research and scientific papers

A Homogeneous Method for the Conveniently Scalable Palladium- and Nickel-Catalyzed Cyanation of Aryl Halides

Burg, Finn,Egger, Julian,Deutsch, Johannes,Guimond, Nicolas

, p. 1540 - 1545 (2016/08/30)

Homogeneous conditions for the palladium-catalyzed cyanation of aryl halides were developed. This new system features a broad scope of aryl chlorides and bromides, uses 2-propanol or 1-butanol as solvent, and is readily scalable. The same conditions can also provide simple benzonitriles using the recently developed (TMEDA)NiCl(o-tolyl) precatalyst in conjunction with 1,1′-bis(diphenylphosphino)ferrocene (dppf) as a ligand.

Physical gelation of polar aprotic solvents induced by hydrogen bonding modulation of polymeric molecules

Ka, Duyoun,Seo, Myungeun,Choi, Hyungsam,Kim, Eun Hee,Kim, Sang Youl

supporting information; scheme or table, p. 5722 - 5724 (2010/09/18)

Poly(aryl ether amide) containing o-nitroanilide forms a physical gel in polar aprotic solvents by solvent-induced change of hydrogen bonding modes, in which hydrogen bonding acceptor solvent molecules break intramolecular hydrogen bonding of o-nitroanili

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