372-20-3

  • Product Name:3-Fluorophenol
  • Molecular Formula:C6H5FO
  • Purity:99%
  • Molecular Weight:112.104
Inquiry

Product Details;

CasNo: 372-20-3

Molecular Formula: C6H5FO

Appearance: colourless to light yellow liquid

99% Pure Factory Supply 3-Fluorophenol 372-20-3 Reasonable Price

  • Molecular Formula:C6H5FO
  • Molecular Weight:112.104
  • Appearance/Colour:colourless to light yellow liquid 
  • Vapor Pressure:0.749mmHg at 25°C 
  • Melting Point:8-12 °C(lit.) 
  • Refractive Index:n20/D 1.514(lit.)  
  • Boiling Point:178 °C at 760 mmHg 
  • PKA:9.29(at 25℃) 
  • Flash Point:71.1 °C 
  • PSA:20.23000 
  • Density:1.217 g/cm3 
  • LogP:1.53130 

3-Fluorophenol(Cas 372-20-3) Usage

Chemical Properties

colourless to light yellow liquid

Uses

3-Fluorophenol is a reactant used in organic synthesis.

InChI:InChI=1/C6H5FO/c7-5-2-1-3-6(8)4-5/h1-4,8H

372-20-3 Relevant articles

Process development and manufacture of potassium 2-fluoro-6-hydroxyphenyltrifluoroborate

Pawar, Lokesh,Jayaramaiah, Ramesh,Krishnan, Baburaj,Arunachalampillai, Athimoolam,Chen, Ying,Parsons, Andrew T.,Robinson, Jo Anna,Tedrow, Jason S.

, p. 4266 - 4270 (2019)

The development of a phase-appropriate m...

Synthesis method of fluorine-containing phenol structure compound

-

Paragraph 0033-0034, (2021/03/13)

The invention discloses a synthesis meth...

A mild and practical method for deprotection of aryl methyl/benzyl/allyl ethers with HPPh2andtBuOK

Pan, Wenjing,Li, Chenchen,Zhu, Haoyin,Li, Fangfang,Li, Tao,Zhao, Wanxiang

, p. 7633 - 7640 (2021/09/22)

A general method for the demethylation, ...

Method for hydrolyzing diarylether compound to generate aryl phenol compound

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Paragraph 0146-0149, (2021/09/29)

The invention discloses a method for hyd...

Nickel Hydride Catalyzed Cleavage of Allyl Ethers Induced by Isomerization

Kathe, Prasad M.,Berkefeld, Andreas,Fleischer, Ivana

supporting information, p. 1629 - 1632 (2021/02/09)

This report discloses the deallylation o...

372-20-3 Process route

2-(3-fluorophenoxy)benzonitrile

2-(3-fluorophenoxy)benzonitrile

salicylonitrile
611-20-1

salicylonitrile

3-fluorophenol
372-20-3

3-fluorophenol

Conditions
Conditions Yield
With uranyl(VI) nitrate monohydrate; water; trichloroacetic acid; at -78 - 25 ℃; for 72h; Irradiation; Inert atmosphere;
 
fluorobenzene
462-06-6

fluorobenzene

4-Fluorophenol
371-41-5

4-Fluorophenol

3-fluorophenol
372-20-3

3-fluorophenol

2-fluorophenol
367-12-4

2-fluorophenol

Conditions
Conditions Yield
With VO(O2)(picolinato)(H2O)2; In acetonitrile; at 20 ℃; Product distribution; Mechanism; dependence on initial conc. of the substrate;
 
With Pt/titania; water; for 3h; Reagent/catalyst; Wavelength; regioselective reaction; Reactivity; Photolysis;
 
With [Fe(II)(bpmen)(CH3CN)2](ClO4)2; dihydrogen peroxide; In acetonitrile; at 20 ℃;
 
fluorobenzene; With formic acid; CoO40W12(5-)*16H2O*5K(1+); lithium formate; at 25 ℃; for 3h; Electrochemical reaction;
With perchloric acid; In diethyl ether; water; at 20 ℃; for 0.166667h;
 

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