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162515

Sigma-Aldrich

2-Fluorobenzyl alcohol

98%

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About This Item

Linear Formula:
FC6H4CH2OH
CAS Number:
446-51-5
Molecular Weight:
126.13
Beilstein/REAXYS Number:
2079486
EC Number:
207-170-7
MDL number:
MFCD00004601
UNSPSC Code:
12352100
PubChem Substance ID:
24849987
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.514 (lit.)

density

1.173 g/mL at 25 °C (lit.)

functional group

fluoro
hydroxyl

SMILES string

OCc1ccccc1F

InChI

1S/C7H7FO/c8-7-4-2-1-3-6(7)5-9/h1-4,9H,5H2

InChI key

QEHXDOJPVIHUDO-UHFFFAOYSA-N

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assay

98%

assay

98%

assay

98%

assay

95%

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

mp

200-202 °C (lit.)

mp

−17-−13 °C (lit.)

mp

135-138 °C (lit.)

mp

122-124 °C (lit.)

General description

2-Fluorobenzyl alcohol undergoes oxidation using graphite oxide under ultrasonic irradiation to yield 2-fluorobenzaldehyde[1].

Application

2-Fluorobenzyl alcohol was used in Nafion-H catalyzed preparation of diphenylmethyl ethers of alcohols[2].

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

194.0 °F - closed cup

flash_point_c

90 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    MKCM4382
    MKCK2623
    MKCC3699
    MKBX3079V
    MKBR9990V

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    Nafion-catalyzed preparation of benzhydryl ethers.
    Stanescu MA and Varma RS.
    Tetrahedron Letters, 43(41), 7307-7309 (2002)
    Graphite oxide: an efficient reagent for oxidation of alcohols under sonication.
    Mirza-Aghayan M, et al.
    Tetrahedron Letters, 53(37), 4962-4965 (2012)
    Rianne E van Outersterp et al.
    The Analyst, 145(18), 6162-6170 (2020-09-15)
    Distinguishing positional isomers, such as compounds having different substitution patterns on an aromatic ring, presents a significant challenge for mass spectrometric analyses and is a frequently encountered difficulty in, for example, drug metabolism research. In contrast to mass spectrometry, IR

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