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Manufacturer supply good quality 2-Fluorobenzyl alcohol 446-51-5 with stock

  • Molecular Formula: C7H7FO
  • Molecular Weight: 126.13
  • Appearance/Colour: Clear colorless to slightly yellow liquid 
  • Vapor Pressure: 1.16mmHg at 25°C 
  • Melting Point: 91-94 °C 
  • Refractive Index: n20/D 1.514(lit.)  
  • Boiling Point: 196.1 °C at 760 mmHg 
  • PKA: 13.88±0.10(Predicted) 
  • Flash Point: 90.6 °C 
  • PSA: 20.23000 
  • Density: 1.173 g/cm3 
  • LogP: 1.31800 

2-Fluorobenzyl alcohol(Cas 446-51-5) Usage

General Description

2-Fluorobenzyl alcohol undergoes oxidation using graphite oxide under ultrasonic irradiation to yield 2-fluorobenzaldehyde.

InChI:InChI=1/C7H5FO/c8-7-4-2-1-3-6(7)5-9/h1-5H

446-51-5 Relevant articles

Pt nanoparticles entrapped in mesoporous metal-organic frameworks MIL-101 as an efficient catalyst for liquid-phase hydrogenation of benzaldehydes and nitrobenzenes

Pan, Huiyan,Li, Xiaohong,Yu, Yin,Li, Junrui,Hu, Jun,Guan, Yejun,Wu, Peng

, p. 1 - 9 (2015)

Metal organic-framework MIL-101 and inor...

Two isomers of a bis(diphenylphosphino)phosphinine, and the synthesis and reactivity of Ru arene/Cp* phosphinophosphinine complexes

Newland, Robert J.,Delve, Matthew P.,Wingad, Richard L.,Mansell, Stephen M.

, p. 19625 - 19636 (2018)

The reaction of 4,6-di(tert-butyl)-1,3,2...

Reaction of Diisobutylaluminum Borohydride, a Binary Hydride, with Selected Organic Compounds Containing Representative Functional Groups

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supporting information, p. 6207 - 6227 (2021/05/06)

The binary hydride, diisobutylaluminum b...

Application of bis(phosphinite) pincer nickel complexes to the catalytic hydrosilylation of aldehydes

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, (2020/10/27)

A series of bis(phosphinite) (POCOP) pin...

Generation of Oxidoreductases with Dual Alcohol Dehydrogenase and Amine Dehydrogenase Activity

Tseliou, Vasilis,Schilder, Don,Masman, Marcelo F.,Knaus, Tanja,Mutti, Francesco G.

supporting information, p. 3315 - 3325 (2020/12/11)

The l-lysine-?-dehydrogenase (LysEDH) fr...

Synthesis, Docking, and Biological activities of novel Metacetamol embedded [1,2,3]-triazole derivatives

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446-51-5 Process route

2-Fluorobenzaldehyde
446-52-6

2-Fluorobenzaldehyde

2-fluorobenzyl alcohol
446-51-5

2-fluorobenzyl alcohol

o-fluoro-benzoic acid
445-29-4

o-fluoro-benzoic acid

Conditions
Conditions Yield
With sodium hydroxide; In water; at 25 ℃; for 3.5h;
90%
With barium dihydroxide; formaldehyd; at 100 - 110 ℃; for 0.166667h;
1 % Chromat.
90 % Chromat.
With 1-hydrosilatrane; sodium hydroxide; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;
46 %Spectr.
2-Fluorobenzaldehyde; In neat (no solvent); for 0.0333333h; Green chemistry;
With 1,4-diaza-bicyclo[2.2.2]octane; In neat (no solvent); at 40 ℃; for 0.00416667h; Reagent/catalyst; Microwave irradiation; Green chemistry;
2-Fluorotoluene
95-52-3

2-Fluorotoluene

2-fluorobenzyl alcohol
446-51-5

2-fluorobenzyl alcohol

2-Fluorobenzaldehyde
446-52-6

2-Fluorobenzaldehyde

o-fluoro-benzoic acid
445-29-4

o-fluoro-benzoic acid

Conditions
Conditions Yield
2-Fluorotoluene; With C40H32CoN8; at 185 ℃; under 12751.3 Torr;
With water; at 144 ℃; under 9000.9 Torr;

446-51-5 Upstream products

  • 446-48-0
    446-48-0

    o-fluorobenzyl bromide

  • 95-52-3
    95-52-3

    2-Fluorotoluene

  • 102606-96-2
    102606-96-2

    2-fluorobenzyl acetate

  • 64-17-5
    64-17-5

    ethanol

446-51-5 Downstream products

  • 446-48-0
    446-48-0

    o-fluorobenzyl bromide

  • 128595-02-8
    128595-02-8

    2-fluorobenzyl N-succinimidyl carbonate

  • 345-35-7
    345-35-7

    2-fluorobenzyl chloride

  • 446-52-6
    446-52-6

    2-Fluorobenzaldehyde

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