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367-86-2

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367-86-2 Usage

Chemical Properties

clear yellow liquid

Uses

Different sources of media describe the Uses of 367-86-2 differently. You can refer to the following data:
1. 4-Fluoro-3-nitrobenzotrifluoride is used in the pre-column derivatization technique for HPLC with UV/VIS spectrophotometric detection of polyamines. It may be used as derivatization reagent for the HPLC determination of polyamines. It was also used in the synthesis of 2-nitro-4-trifluoromethylphenylhydrazine, derivatization reagent for 1,2-diol compounds and oxo-steroids. ? [3-(2-nitro-4-trifluoromethylphenyl)aminophenyl]dihydroxyborane, derivatization reagent for 1,2-diol compounds and oxo-steroids3 ? 1-(3-chlorophenyl)-5-trifluoromethyl-3-hydrobenzimidazol-2-one
2. 4-Fluoro-3-nitrobenzotrifluoride was used in pre-column derivatization technique for HPLC with UV/VIS spectrophotometric detection of polyamines. It was also used in the synthesis of:2-nitro-4-trifluoromethylphenylhydrazine, derivatization reagent for 1,2-diol compounds and oxo-steroids[3-(2-nitro-4-trifluoromethylphenyl)aminophenyl]dihydroxyborane, derivatization reagent for 1,2-diol compounds and oxo-steroids1-(3-chlorophenyl)-5-trifluoromethyl-3-hydrobenzimidazol-2-one

Check Digit Verification of cas no

The CAS Registry Mumber 367-86-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 367-86:
(5*3)+(4*6)+(3*7)+(2*8)+(1*6)=82
82 % 10 = 2
So 367-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5F2NO2/c8-4-5-1-2-6(9)7(3-5)10(11)12/h1-3H,4H2

367-86-2 Well-known Company Product Price

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  • Alfa Aesar

  • (A19676)  4-Fluoro-3-nitrobenzotrifluoride, 97%   

  • 367-86-2

  • 25g

  • 309.0CNY

  • Detail
  • Alfa Aesar

  • (A19676)  4-Fluoro-3-nitrobenzotrifluoride, 97%   

  • 367-86-2

  • 100g

  • 697.0CNY

  • Detail
  • Alfa Aesar

  • (A19676)  4-Fluoro-3-nitrobenzotrifluoride, 97%   

  • 367-86-2

  • 500g

  • 2680.0CNY

  • Detail
  • Aldrich

  • (214337)  4-Fluoro-3-nitrobenzotrifluoride  99%

  • 367-86-2

  • 214337-5G

  • 1,042.47CNY

  • Detail
  • Aldrich

  • (346640)  4-Fluoro-3-nitrobenzotrifluoride  96%

  • 367-86-2

  • 346640-100G

  • 540.19CNY

  • Detail

367-86-2SDS

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 4-Fluoro-3-nitrobenzotrifluoride

1.2 Other means of identification

Product number -
Other names 3-NITRO-4-FLUOROBENZOTRIFLUORIDE

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:367-86-2 SDS

367-86-2Relevant articles and documents

Efficient phosphorus catalysts for the halogen-exchange (Halex) reaction

Lacour, Marie-Agnes,Zablocka, Maria,Duhayon, Carine,Majoral, Jean-Pierre,Taillefer, Marc

supporting information; experimental part, p. 2677 - 2682 (2009/10/20)

New families of monomeric to dendritic, and monocationic to multicationic (PNP) compounds have been prepared and tested as catalysts in halogen exchange (Halex) reactions. Some of them allow an increase in the efficiency of these reactions which are performed in some cases under the mildest conditions reported up to now.

THE SYNTHESIS OF ORGANOFLUORINE COMPOUNDS USING POTASSIUM FLUORIDE-TETRAPHENYLPHOSPHONIUM BROMIDE SYSTEMS.

Clark, James H.,Macquarrie, Duncan J.

, p. 111 - 114 (2007/10/02)

The reactivity of potassium fluoride in nucleophilic fluorine transfer reactions can appreciably enhanced by the presence of tetraphenyl phosphonium bromide.Rate accelerations are especially large in non dipolar aprotic solvents.

Thieno[3,2-b]-[1,5]benzodiazepines

-

, (2008/06/13)

Thieno[1,5]benzodiazepines having useful CNS activity containing the novel tricyclic ring system: STR1 the 10-position being substituted by an amino, preferably a piperazino, group.

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