155799
4-Fluorostyrene
99%, contains tert-butylcatechol as inhibitor
Synonym(s):
1-Ethenyl-4-fluorobenzene, 1-Vinyl-4-fluorobenzene, p -Fluorostyrene
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
H2C=CHC6H4F
CAS Number:
Molecular Weight:
122.14
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
206-975-0
Beilstein/REAXYS Number:
1634203
MDL number:
InChI key
JWVTWJNGILGLAT-UHFFFAOYSA-N
InChI
1S/C8H7F/c1-2-7-3-5-8(9)6-4-7/h2-6H,1H2
SMILES string
Fc1ccc(C=C)cc1
assay
99%
form
liquid
contains
tert-butylcatechol as inhibitor
bp
67 °C/50 mmHg (lit.)
density
1.024 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Articles
Fluorocarbon polymers exhibit increased thermal stability, hydrophobicity, lipophobicity, and chemical resistance compared to hydrocarbon analogs.
Related Content
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service