440-60-8

  • Product Name:2,3,4,5,6-Pentafluorobenzyl alcohol
  • Molecular Formula:C7H3F5O
  • Purity:99%
  • Molecular Weight:198.092
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Product Details;

CasNo: 440-60-8

Molecular Formula: C7H3F5O

Appearance: white crystalline mass

factory and supplier 440-60-8 2,3,4,5,6-Pentafluorobenzyl alcohol in stock

  • Molecular Formula:C7H3F5O
  • Molecular Weight:198.092
  • Appearance/Colour:white crystalline mass 
  • Vapor Pressure:0.115mmHg at 25°C 
  • Melting Point:37-38 °C(lit.) 
  • Refractive Index:1.487 
  • Boiling Point:181 °C at 760 mmHg 
  • PKA:13.07±0.10(Predicted) 
  • Flash Point:87.8 °C 
  • PSA:20.23000 
  • Density:1.593 g/cm3 
  • LogP:1.87440 

2,3,4,5,6-Pentafluorobenzyl alcohol(Cas 440-60-8) Usage

Definition

ChEBI: An organofluorine compound that is benzyl alcohol substituted by fluoro groups at positions 2, 3, 4, 5 and 6.

General Description

Structures of complex of horse liver alchohol dehydrogenase enzyme with 2,3,4,5,6-pentafluorobenzyl alcohol has been investigated by X-ray crystallography.

InChI:InChI=1/C9H9FO2/c1-2-12-9(11)7-5-3-4-6-8(7)10/h3-6H,2H2,1H3

440-60-8 Relevant articles

Mono- and Di-Mesoionic Carbene-Boranes: Synthesis, Structures and Utility as Reducing Agents

Stein, Felix,Kirsch, Marius,Beerhues, Julia,Albold, Uta,Sarkar, Biprajit

supporting information, p. 2417 - 2424 (2021/06/17)

Mesoionic carbenes (MIC) of the 1,2,3-tr...

Chemoselective and Site-Selective Reductions Catalyzed by a Supramolecular Host and a Pyridine-Borane Cofactor

Morimoto, Mariko,Cao, Wendy,Bergman, Robert G.,Raymond, Kenneth N.,Toste, F. Dean

supporting information, p. 2108 - 2114 (2021/02/06)

Supramolecular catalysts emulate the mec...

Copper(II)-Catalyzed Selective Hydroboration of Ketones and Aldehydes

Zeng, Haisu,Wu, Jing,Li, Sihan,Hui, Christina,Ta, Anita,Cheng, Shu-Yuan,Zheng, Shengping,Zhang, Guoqi

, p. 401 - 406 (2019/01/23)

A novel nonanuclear copper(II) complex o...

Method for preparing polyfluorobenzyl alcohol

-

Paragraph 0039; 0040, (2018/05/16)

The invention relates to a method for pr...

440-60-8 Process route

perfluorobenzaldehyde
653-37-2

perfluorobenzaldehyde

(2,3,4,5,6-pentafluorophenyl)methanol
440-60-8

(2,3,4,5,6-pentafluorophenyl)methanol

Conditions
Conditions Yield
perfluorobenzaldehyde; With C24H20Cl2F5NRuS; isopropyl alcohol; at 82 ℃; for 0.166667h;
With potassium hydroxide; at 82 ℃; for 0.5h;
100%
With sodium tetrahydroborate; 1,4,8,11,15,18,22,25-octapentyloxyphthalocyaninato nickel; In pentan-1-ol; at 25 ℃; for 0.416667h; Catalytic behavior;
87%
With tris(pentafluorophenyl)borate; hydrogen; In 1,4-dioxane; at 80 ℃; for 24h; under 3750.38 Torr; Glovebox; Inert atmosphere;
74%
With glucose dehydrogenase; D-glucose; Bacteroides fragilis ATCC 25285 7α-hydroxysteroid dehydrogenase; NAD; In dimethyl sulfoxide; at 30 ℃; for 42h; pH=7; aq. phosphate buffer; Enzymatic reaction;
72%
With lithium aluminium tetrahydride;
With Dimethylphenylsilane; o-phenylenebis(diphenylphosphine); potassium tert-butylate; copper(l) chloride; In tetrahydrofuran; for 12h; regioselective reaction; Inert atmosphere; Reflux;
With D-glucose; D-glucose dehydrogenase; a putative aldehyde reductase (OsAR) from Oceanospirillum sp.MED92; NADPH; In aq. phosphate buffer; at 25 ℃; for 18h; pH=6.5; chemoselective reaction; Enzymatic reaction;
Multi-step reaction with 2 steps
1: C27H44AlN3 / 0.33 h / 20 °C / Inert atmosphere; Glovebox
2: silica gel / Inert atmosphere; Heating
With C27H44AlN3; silica gel;
With C40H46ClN2OPRu(2+)*F6P(1-)*Cl(1-); sodium formate; In water; at 80 ℃; for 5h; Catalytic behavior; Inert atmosphere; Schlenk technique;
97 %Chromat.
Multi-step reaction with 2 steps
1: C74H94Cu9N4O28 / neat (no solvent) / 1 h / 20 °C / Glovebox; Inert atmosphere
2: silica gel / ethyl acetate; hexane / 20 °C
With C74H94Cu9N4O28; silica gel; In hexane; ethyl acetate;
With C21H28BN3; silica gel; In dichloromethane; at 20 ℃; for 3h; Inert atmosphere; Schlenk technique;
35 %Spectr.
2,3,4,5,6-pentafluorobenzoic anhydride
15989-99-8

2,3,4,5,6-pentafluorobenzoic anhydride

(2,3,4,5,6-pentafluorophenyl)methanol
440-60-8

(2,3,4,5,6-pentafluorophenyl)methanol

Conditions
Conditions Yield
With sodium tetrahydroborate; In ethanol; for 1h;
98%

440-60-8 Upstream products

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    2,3,4,5,6-pentafluorobenzylamine

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440-60-8 Downstream products

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    121720-32-9

    C22H17F5O2

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