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Safety Information

155799

Sigma-Aldrich

4-Fluorostyrene

99%, contains tert-butylcatechol as inhibitor

Synonym(s):

1-Ethenyl-4-fluorobenzene, 1-Vinyl-4-fluorobenzene, p -Fluorostyrene

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About This Item

Linear Formula:
H2C=CHC6H4F
CAS Number:
405-99-2
Molecular Weight:
122.14
Beilstein:
1634203
EC Number:
206-975-0
MDL number:
MFCD00000361
UNSPSC Code:
12162002
PubChem Substance ID:
24849567
NACRES:
NA.23

Assay

99%

form

liquid

contains

tert-butylcatechol as inhibitor

refractive index

n20/D 1.514 (lit.)

bp

67 °C/50 mmHg (lit.)

density

1.024 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

Fc1ccc(C=C)cc1

InChI

1S/C8H7F/c1-2-7-3-5-8(9)6-4-7/h2-6H,1H2

InChI key

JWVTWJNGILGLAT-UHFFFAOYSA-N

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Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

95.0 °F - closed cup

Flash Point(C)

35 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCC6671
MKBW3852V
MKBK9200V
MKBB3010
05606TH

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Christoph Sprung et al.
Journal of the American Chemical Society, 137(5), 1916-1928 (2015-01-16)
A detailed and systematic polarized confocal fluorescence microscopy investigation is presented on three batches of large coffin-shaped ZSM-5 crystals (i.e., parent, steamed at 500 °C, and steamed at 700 °C). In total, six laser lines of different wavelength in the
Oriol Planas et al.
Science (New York, N.Y.), 367(6475), 313-317 (2020-01-18)
Bismuth catalysis has traditionally relied on the Lewis acidic properties of the element in a fixed oxidation state. In this paper, we report a series of bismuth complexes that can undergo oxidative addition, reductive elimination, and transmetallation in a manner
Christopher L Rock et al.
Dalton transactions (Cambridge, England : 2003), 48(2), 461-467 (2018-11-30)
The phosphine-substituted α-diimine Ni precursor, (Ph2PPrDI)Ni, has been found to catalyze alkene hydrosilylation in the presence of Ph2SiH2 with turnover frequencies of up to 124 h-1 at 25 °C (990 h-1 at 60 °C). Moreover, the selective hydrosilylation of allylic

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