Intermediate of API

99627-05-1

  • Product Name：3,4,5-Trifluorophenol
  • Molecular Formula：C6H3F3O
  • Specifications：99%
  • Molecular Weight：148.084
Inquiry

Product Details;

CasNo： 99627-05-1

Molecular Formula： C6H3F3O

Appearance： white to light yellow crystal powder

High Quality 3,4,5-Trifluorophenol 99627-05-1 Powder In Bulk Supply

  • Molecular Formula:C6H3F3O
  • Molecular Weight:148.084
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:0.238mmHg at 25°C 
  • Melting Point:52-55 °C 
  • Refractive Index:1.471 
  • Boiling Point:199.7 °C at 760 mmHg 
  • PKA:8.00±0.23(Predicted) 
  • Flash Point:86.3 °C 
  • PSA：20.23000 
  • Density:1.473 g/cm3 
  • LogP:1.80950 

3,4,5-Trifluorophenol(Cas 99627-05-1) Usage

Chemical Properties

white to light yellow crystal powder

Uses

3,4,5-Trifluorophenol may be used in the synthesis of 3,4,5-trifluorophenoxymethyl-substituted polystyrene.

General Description

3,4,5-Trifluorophenol is a halo-substituted phenol. It participates in the synthesis of difluorooxymethylene-bridged liquid crystals.

Flammability and Explosibility

Notclassified

InChI:InChI=1/C6H3F3O/c7-4-1-3(10)2-5(8)6(4)9/h1-2,10H

99627-05-1 Relevant articles

Improved synthesis technology of 3,4,5-trifluorophenol

-

Paragraph 0041-0043, (2020/04/29)

The invention discloses a synthesis tech...

Synthesis method of 3, 4, 5-trifluorophenol

-

Paragraph 0038-0061, (2019/03/28)

The invention discloses a synthesis meth...

A practical method for preparation of phenols from arylboronic acids catalyzed by iodopovidone in aqueous medium

Dong, Bin,Ke, Yanxiong,Lu, Guangying,Ren, Jiangmeng,Ren, Yaoyao,Zeng, Bu-Bing,Zhou, Bin

, (2019/09/06)

A novel and efficient strategy for the i...

Preparation method of fluorine-containing phenol

-

, (2017/08/29)

The invention provides a preparation met...

99627-05-1 Process route

3,4,5-trifluoro-1-bromobenzene
138526-69-9

3,4,5-trifluoro-1-bromobenzene

3,4,5-trifluorophenol
99627-05-1

3,4,5-trifluorophenol

Conditions
Conditions Yield
With sulfolane; potassium hydroxide; In water; at 150 ℃; for 10h; under 7500.75 Torr; Inert atmosphere; Autoclave;
81.3%
Multi-step reaction with 2 steps
1: 1,10-Phenanthroline; copper(I) bromide; potassium carbonate / 5 h / 80 °C / Inert atmosphere
2: sulfuric acid / water / 2 h / 90 °C
With 1,10-Phenanthroline; sulfuric acid; potassium carbonate; copper(I) bromide; In water;
3,4,5-trifluoro aniline
163733-96-8

3,4,5-trifluoro aniline

3,4,5-trifluorophenol
99627-05-1

3,4,5-trifluorophenol

Conditions
Conditions Yield
3,4,5-trifluoro aniline; With nitrosylsulfuric acid; sulfuric acid; In water; at -5 - 70 ℃; for 1.5h; Autoclave;
With sulfuric acid; copper(II) sulfate; In water; Solvent; Reagent/catalyst; Reflux;
90.2%

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