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2822-41-5

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2822-41-5 Usage

Chemical Properties

clear colorless to slightly yellow liquid

Uses

2,3,4-Trifluorophenol can be used as a supported catalyst for olefin polymerization and load methods. It can also be used as a resin compound for cladding of optical fiber.

General Description

2,3,4-Trifluorophenol is an ortho-fluorinated trifluorophenol. Biodegradation and oxidative biodehalogenation of 2,3,4-trifluorophenol has been studied by 19F nuclear magnetic resonance (NMR) spectra.

Check Digit Verification of cas no

The CAS Registry Mumber 2822-41-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2822-41:
(6*2)+(5*8)+(4*2)+(3*2)+(2*4)+(1*1)=75
75 % 10 = 5
So 2822-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H3F3O/c7-3-1-2-4(10)6(9)5(3)8/h1-2,10H

2822-41-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Price
  • Detail
  • Alfa Aesar

  • (B20142)  2,3,4-Trifluorophenol, 98%   

  • 2822-41-5

  • 1g

  • 547.0CNY

  • Detail
  • Alfa Aesar

  • (B20142)  2,3,4-Trifluorophenol, 98%   

  • 2822-41-5

  • 5g

  • 1991.0CNY

  • Detail

2822-41-5SDS

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 2,3,4-TRIFLUOROPHENOL

1.2 Other means of identification

Product number -
Other names Phenol,2,3,4-trifluoro

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:2822-41-5 SDS

2822-41-5Relevant articles and documents

Nucleophilicity vs. basicity of the hydroxide ion under extractive phase transfer catalysis conditions

Feldman,Rabinovitz

, p. 6091 - 6094 (1989)

Extraction of hydroxide ion under phase transfer catalysis conditions (PTC) affords an extremely strong base and nucleophile. The competition between H/D exchange and nucleophilic aromatic substitution on 1,2,3,4-Tetrafluorobenzene shows that under extractive phase transfer catalysis conditions the hydroxide ion is more effective as a base than as a nucleophile.

Method for production of 2,3,4,5-tetrafluorobenzoic acid

-

, (2008/06/13)

A method for the production of 2,3,4,5-tetrafluorobenzoic acid, which comprises effecting said production by decarbonating 3,4,5,6-tetrafluorophthalic acid in an aqueous medium adjusted to a pH in the range of 0.7 to 2.2 at a temperature in the range of 100° to 220° C.

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