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Key Documents

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196746

Sigma-Aldrich

2,3,4,5,6-Pentafluorobenzyl alcohol

98%

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About This Item

Fórmula lineal:
C6F5CH2OH
Número de CAS:
440-60-8
Peso molecular:
198.09
EC Number:
207-126-7
MDL number:
MFCD00004602
UNSPSC Code:
12352100
PubChem Substance ID:
24851790
NACRES:
NA.22

assay

98%

form

solid

bp

114-115 °C/60 mmHg (lit.)

mp

37-38 °C (lit.)

SMILES string

OCc1c(F)c(F)c(F)c(F)c1F

InChI

1S/C7H3F5O/c8-3-2(1-13)4(9)6(11)7(12)5(3)10/h13H,1H2

InChI key

PGJYYCIOYBZTPU-UHFFFAOYSA-N

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.

Application

2,3,4,5,6-Pentafluorobenzyl alcohol was used in the synthesis of pentafluorobenzyloxy substituted metal-free phthalocyanine.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

190.4 °F - closed cup

flash_point_c

88 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

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Iodopentafluorobenzene 99%

Sigma-Aldrich

103136

Iodopentafluorobenzene

C Oman
Environmental science & technology, 35(1), 232-239 (2001-05-16)
Emissions of organic compounds from landfills depend on the fate of the compounds inside the landfills. This field study was used to investigate the fate in landfills of organic compounds having different physical, chemical, and biological characteristics. For this purpose
Jon K Rubach et al.
Biochemistry, 41(52), 15770-15779 (2002-12-27)
The relationship between substrate mobility and catalysis was studied with wild-type and Phe93Ala (F93A) horse liver alcohol dehydrogenase (ADH). Wild-type ADH binds 2,3,4,5,6-pentafluorobenzyl alcohol in one position as shown by X-ray results, and (19)F NMR shows five resonances for the
H Eklund et al.
EXS, 71, 269-277 (1994-01-01)
The structures of horse liver alcohol dehydrogenase class I in its apoenzyme form and in different ternary complexes have been determined at high resolution. The complex with NAD+ and the substrate analogue pentafluorobenzyl alcohol gives a detailed picture of the
Novel phthalocyanines with pentafluorobenzyloxy-substituents.
Selcukoglu M and Hamuryudan E.
Dyes and Pigments, 74(1), 17-20 (2007)
V G Voinov et al.
Analytical chemistry, 76(10), 2951-2957 (2004-05-18)
A prototype gas chromatograph (GC) electron monochromator (EM) reflectron time-of-flight (TOF) mass spectrometer has been constructed and demonstrated to simultaneously record four-dimensional resonant electron capture (REC) mass spectra (m/z, ion-intensity, electron-energy, and retention time) of electron-capturing compounds in real time.
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