4-Vinylbenzoic Acid

Product Information

Molecular Formula:
C9H8O2
Molecular Weight:
148.16
Description
4-Vinylbenzoic Acid (CAS# 1075-49-6) is a useful research chemical.
Synonyms
4-ethenylbenzoic acid; 4-ethenylbenzoic acid
IUPAC Name
4-ethenylbenzoic acid
Canonical SMILES
C=CC1=CC=C(C=C1)C(=O)O
InChI
InChI=1S/C9H8O2/c1-2-7-3-5-8(6-4-7)9(10)11/h2-6H,1H2,(H,10,11)
InChI Key
IRQWEODKXLDORP-UHFFFAOYSA-N
Boiling Point
228.74 ℃ (rough estimate)
Melting Point
142-144 ℃ (lit.)
Purity
> 97.0 % (GC) (T)
Density
1.30 g/cm3
Appearance
White to light yellow powder to crystal
Storage
0-10 ℃
Refractive Index
1.5290 (estimate)
LogP
2.02780

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
2.7
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
2
Exact Mass
148.052429494 g/mol
Monoisotopic Mass
148.052429494 g/mol
Topological Polar Surface Area
37.3Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
155
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114106225-A Dispersant for eliminating amplification effect and preparation method thereof 2021-12-17
JP-2022040139-A Polishing liquid, polishing liquid set and polishing method 2021-12-17
JP-2022040133-A A photosensitive coloring composition for a color filter for a solid-state image sensor, a color filter, and a solid-state image sensor using the same. 2021-12-15
CN-114163579-A Viscosity-reducing water-retaining polycarboxylate superplasticizer and preparation method thereof 2021-11-25
CN-114181355-A Ester-ether mixed viscosity-reducing polycarboxylate superplasticizer and preparation method thereof 2021-11-25
CN-114113394-A Magnetic microsphere for extracting and purifying paraquat metabolite, preparation method, kit and extraction method 2021-11-24
CN-114163565-A Method for extracting nicotine from molecularly imprinted polymer 2021-11-22
CN-113648782-A Carbon dioxide recovery device and carbon dioxide recovery method 2021-10-19
CN-113648782-B Carbon dioxide recovery device and carbon dioxide recovery method 2021-10-19
CN-113634087-A Method and device for obtaining CO2 from outlet of oil production well in carbon dioxide oil production method 2021-10-18

Literatures

PMID Publication Date Title Journal
23009188 2012-10-16 Rate determination of azide click reactions onto alkyne polymer brush scaffolds: a comparison of conventional and catalyst-free cycloadditions for tunable surface modification Langmuir : the ACS journal of surfaces and colloids
22461424 2012-06-01 Photocurrent enhancement of dye-sensitized solar cells owing to increased dye-adsorption onto silicon-nanoparticle-coated titanium-dioxide films Chemistry, an Asian journal
21866918 2011-10-18 Miniemulsion synthesis of metal-oxo cluster containing copolymer nanobeads Langmuir : the ACS journal of surfaces and colloids
20099926 2010-02-02 High density scaffolding of functional polymer brushes: surface initiated atom transfer radical polymerization of active esters Langmuir : the ACS journal of surfaces and colloids
19453166 2009-07-13 Synthesis of polymerizable protein monomers for protein-acrylamide hydrogel formation Biomacromolecules
19582213 2009-05-26 An updated review of tyrosinase inhibitors International journal of molecular sciences
19260656 2009-04-21 Complex adsorption behavior of rodlike polyelectrolyte-surfactant aggregates Langmuir : the ACS journal of surfaces and colloids
19243090 2009-04-13 RAFT synthesis and stimulus-induced self-assembly in water of copolymers based on the biocompatible monomer 2-(methacryloyloxy)ethyl phosphorylcholine Biomacromolecules
18762195 2008-11-14 Crystal structure of CYP199A2, a para-substituted benzoic acid oxidizing cytochrome P450 from Rhodopseudomonas palustris Journal of molecular biology
19202869 2008-01-01 Chlorobenzene degradation by electro-heterogeneous catalysis in aqueous solution: intermediates and reaction mechanism Journal of environmental sciences (China)
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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