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1,2,3,5-Tetrafluoro-4-trifluoromethyl-benzene, with the molecular formula C7H2F7, is a fluorinated aromatic compound characterized by its unique properties such as high thermal stability and resistance to chemical reactions. Its structure, which includes both fluorine and trifluoromethyl groups, makes it a valuable intermediate in the synthesis of various organic compounds, particularly for the development of new materials and drugs.

5360-82-7

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5360-82-7 Usage

Uses

Used in Pharmaceutical Industry:
1,2,3,5-Tetrafluoro-4-trifluoromethyl-benzene is used as a building block in the synthesis of pharmaceuticals for its unique properties that contribute to the development of new drugs with enhanced efficacy and stability.
Used in Agrochemical Industry:
In the agrochemical sector, 1,2,3,5-Tetrafluoro-4-trifluoromethyl-benzene serves as a key intermediate in the production of agrochemicals, aiding in the creation of compounds that can improve crop protection and yield.
Used in Electronic Materials Industry:
1,2,3,5-TETRAFLUORO-4-TRIFLUOROMETHYL-BENZENE is utilized as a component in the manufacturing of electronic materials, leveraging its thermal stability and chemical resistance to produce materials with superior performance in electronic devices and components.
Used as a Solvent in Industrial Processes:
Due to its favorable physical and chemical properties, 1,2,3,5-Tetrafluoro-4-trifluoromethyl-benzene is also employed as a solvent in certain industrial processes, where its characteristics can enhance the efficiency and effectiveness of these processes.

Check Digit Verification of cas no

The CAS Registry Mumber 5360-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5360-82:
(6*5)+(5*3)+(4*6)+(3*0)+(2*8)+(1*2)=87
87 % 10 = 7
So 5360-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C7HF7/c8-2-1-3(9)5(10)6(11)4(2)7(12,13)14/h1H

5360-82-7SDS

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 1,2,3,5-tetrafluoro-4-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 5-H-heptafluorotoluene

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:5360-82-7 SDS

5360-82-7Downstream Products

5360-82-7Relevant academic research and scientific papers

Organozinc reagents from polyfluoroarenes: Preparation and reactions with allyl halides. Synthesis of allylpolyfluoroarenes

Vinogradov,Krasnov,Platonov

, p. 95 - 102 (2008/12/21)

Organozinc compounds of the general formula ArFZnX (X = Cl, ArF) were synthesized by reactions of Zn with chloropolyfluoroarenes and of Zn/SnCl2 with polyfluoroarenes. Polyflorinated organozinc compounds reacted with allyl

Preparation of organozinc compounds from 3-chloroheptafluorotoluene and zinc: The participation of C-F bonds

Krasnov, Vyacheslav I.,Vinogradov, Andrey S.,Platonov, Vyacheslav E.

, p. 168 - 170 (2007/10/03)

Organozinc compounds were obtained from 3-chloroheptafluorotoluene and Zn in DMF; the C-Cl bond is mainly involved in this reaction; the addition of SnCl2 changes the main reaction course in the direction of the participation of the C-F bond (p

Reaction of polyfluoroaromatic compounds with electrophilic agents in the presence of tris(dialkylamino)phosphines: 7. * Replacement of a halogen by hydrogen in halogenopolyfluoroaromatic compounds

Bardin,Pressman

, p. 786 - 788 (2007/10/03)

A method was developed for the replacement of chlorine, bromine, and iodine in halopolyfluoroaromatic compounds by hydrogen under the action of P(NEt2)3 and a proton donor.

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