4-Vinylphenylboronic Acid

Product Information

Molecular Formula:
C8H9O2B
Molecular Weight:
147.97
Description
4-Vinylphenylboronic acid is commonly used in the synthesis of styrene-based organoboron polymers such as vinyl-oligo(fluorene) polymer and boronic ester based self-healing polymer. It can also be used as a precursor in the synthesis of aggregation induced emission (AIE) dye.
Synonyms
(4-ethenylphenyl)boronic acid; (4-ethenylphenyl)boronic acid
IUPAC Name
(4-ethenylphenyl)boronic acid
Canonical SMILES
B(C1=CC=C(C=C1)C=C)(O)O
InChI
InChI=1S/C8H9BO2/c1-2-7-3-5-8(6-4-7)9(10)11/h2-6,10-11H,1H2
InChI Key
QWMJEUJXWVZSAG-UHFFFAOYSA-N
Boiling Point
306.2±35.0 ℃ (Predicted)
Melting Point
190-193 ℃
Flash Point
Not applicable
Purity
97.0-114.0 %
Density
1.09 g/cm3
Appearance
White to almost white powder to crystal
Storage
Refrigerator (+4 ℃)
LogP
0.00940

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
2
Exact Mass
148.0695597 g/mol
Monoisotopic Mass
148.0695597 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
128
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-114163565-A Method for extracting nicotine from molecularly imprinted polymer 2021-11-22
CN-113980369-A Production process of antibacterial medical gloves 2021-11-15
CN-114011374-A Non-evaporable titanium-molybdenum getter capable of rapidly absorbing air 2021-11-03
CN-113828305-A Preparation method of Pd/attapulgite catalyst for cross-coupling reaction 2021-10-11
CN-113873748-A Circuit board of transparent LED display screen and manufacturing process 2021-09-28
CN-113637327-A High-temperature-resistant silicon rubber sealing ring and preparation method thereof 2021-09-26
CN-113683474-A Method for synthesizing norbornane compound 2021-08-31
CN-113861188-A Pyrazolo [3,4-b ] pyridine derivative, preparation method thereof and application thereof as HPK1 inhibitor 2021-08-23
CN-113292671-A Polymer crosslinking agent containing phenylboronic acid group, biological adhesive prepared from polymer crosslinking agent, and preparation method and application of biological adhesive 2021-07-08
CN-113402664-A Preparation method and application of ginsenoside Rg1 molecularly imprinted polymeric material 2021-07-04

Literatures

PMID Publication Date Title Journal
22888741 2012-10-01 Synthesis and characterization of thermally and glucose-sensitive poly N-vinylcaprolactam-Based microgels Journal of biomedical nanotechnology
22967628 2012-09-15 Synthesis of water-compatible imprinted polymers of in situ produced fructosazine and 2,5-deoxyfructosazine Talanta
22762957 2012-08-17 Preparation and evaluation of poly(4-vinylphenylboronic acid-co-pentaerythritol triacrylate) monolithic column for capillary liquid chromatography of small molecules and proteins Journal of chromatography. A
22425210 2012-07-13 Monolithic column based on a poly(glycidyl methacrylate-co-4-vinylphenylboronic acid-co-ethylene dimethacrylate) copolymer for capillary liquid chromatography of small molecules and proteins Journal of chromatography. A
21799960 2011-09-14 One-pot synthesis of an organic-inorganic hybrid affinity monolithic column for specific capture of glycoproteins Chemical communications (Cambridge, England)
21738938 2011-08-21 Preparation and evaluation of a phenylboronate affinity monolith for selective capture of glycoproteins by capillary liquid chromatography The Analyst
21466557 2011-07-01 Luminescent lanthanide (Eu3+, Tb3+) hybrids with 4-vinylbenzeneboronic acid functionalized Si-O bridges and beta-diketones Photochemistry and photobiology
20732713 2010-12-01 The biological performance of cell-containing phospholipid polymer hydrogels in bulk and microscale form Biomaterials
20235269 2010-05-03 SnO2@Poly(HEMA-co-St-co-VPBA) core-shell nanoparticles designed for selectively enriching glycopeptides followed by MALDI-MS analysis Chemistry, an Asian journal
19850296 2009-11-20 Synthesis of hydrophilic boronate affinity monolithic capillary for specific capture of glycoproteins by capillary liquid chromatography Journal of chromatography. A
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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