
372-20-3
- Product Name:3-Fluorophenol
- Molecular Formula:C6H5FO
- Purity:99%
- Molecular Weight:112.104
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
-
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
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-
2-(3-fluorophenoxy)benzonitrile

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- 611-20-1
salicylonitrile

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- 372-20-3
3-fluorophenol
Conditions | Yield |
---|---|
With uranyl(VI) nitrate monohydrate; water; trichloroacetic acid; at -78 - 25 ℃; for 72h; Irradiation; Inert atmosphere;
|
-
- 462-06-6
fluorobenzene

-
- 371-41-5
4-Fluorophenol

-
- 372-20-3
3-fluorophenol

-
- 367-12-4
2-fluorophenol
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;
|
372-20-3 Upstream products
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372-19-0
meta-fluoroaniline
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456-49-5
1-fluoro-3-methoxybenzene
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1-ethoxy-3-fluorobenzene
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591-27-5
m-Hydroxyaniline
372-20-3 Downstream products
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326-18-1
3-fluoro-4-phenylazo-phenol
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405-25-4
3-fluoro-4-(4-nitro-phenylazo)-phenol
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404-67-1
3-fluoro-4-(3-nitro-phenylazo)-phenol
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331-71-5
1,3-bis-(3-fluoro-phenoxy)-propan-2-ol
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