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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 Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

155799-VAR:
155799-BULK:
155799-10G:
155799-1G:

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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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