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193533-92-5

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193533-92-5 Usage

Description

2,3,4-Trifluorotoluene is an organic compound with the molecular formula C7H5F3. It is a colorless to light yellow liquid that is formed through the corona discharge of 2,3,4-trifluorotoluene, which generates difluorobenzyl radicals. These radicals have been investigated through vibronically well-resolved emission spectra.

Uses

1. Used in Chemical Synthesis:
2,3,4-Trifluorotoluene is used as a building block for the synthesis of various fluorinated organic compounds. Its unique structure and reactivity make it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.
2. Used in Material Science:
In the field of material science, 2,3,4-trifluorotoluene is utilized as a precursor for the development of advanced materials with specific properties, such as enhanced thermal stability, chemical resistance, and improved mechanical strength.
3. Used in Pharmaceutical Industry:
2,3,4-Trifluorotoluene is employed as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those with fluorinated structures. These compounds often exhibit improved pharmacokinetic and pharmacodynamic properties, leading to better drug efficacy and safety profiles.
4. Used in Agrochemical Industry:
In the agrochemical industry, 2,3,4-trifluorotoluene is used as a starting material for the development of novel pesticides and herbicides with enhanced selectivity, reduced environmental impact, and improved efficacy against target pests.
5. Used in Fluoropolymer Production:
2,3,4-Trifluorotoluene serves as a monomer in the production of fluoropolymers, which are known for their exceptional chemical resistance, thermal stability, and non-stick properties. These polymers find applications in various industries, including automotive, aerospace, electronics, and consumer goods.

Check Digit Verification of cas no

The CAS Registry Mumber 193533-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,5,3 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193533-92:
(8*1)+(7*9)+(6*3)+(5*5)+(4*3)+(3*3)+(2*9)+(1*2)=155
155 % 10 = 5
So 193533-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H5F3/c1-4-2-3-5(8)7(10)6(4)9/h2-3H,1H3

193533-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-trifluoro-4-methylbenzene

1.2 Other means of identification

Product number -
Other names alfa,,alfa,,alfa,-trifluorotoluene

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:193533-92-5 SDS

193533-92-5Relevant articles and documents

Friedel–Crafts Type Methylation with Dimethylhalonium Salts

H?mmerling, Sebastian,Vo?nacker, Patrick,Steinhauer, Simon,Beckers, Helmut,Riedel, Sebastian

, p. 14377 - 14384 (2020)

The dimethylchloronium salt [Me2Cl][Al(OTeF5)4] is used to methylate electron-deficient aromatic systems in Friedel–Crafts type reactions as shown by the synthesis of N-methylated cations, such as [MeNC5F5]+, [MeNC5F4I]+, and [MeN3C3F3]+. To gain a better understanding of such fundamental Friedel–Crafts reactions, the role of the dimethylchloronium cation has been evaluated by quantum-chemical calculations.

Novel 5-amino-6-methylquinolone antibacterials: A new class of non-6-fluoroquinolones

Hong, Chang Yong,Kim, Se Ho,Kim, Young Kwan

, p. 1875 - 1878 (2007/10/03)

A novel 5-amino-6-methylquinoline carboxylic acid was synthesized from 2,3,4-trifluoro aniline in 12 steps and coupled with various types of amines to furnish new quinolone antibacterial agents. Depending on the structure of amine, some of quinolones showed comparable activity to ciprofloxacin or better Gram positive activity than ciprofloxacin, demonstrating that the C6 fluorine atom is not a necessary requirement for good antibacterial potency.

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