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
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 °C (Predicted)
Melting Point
190-193 °C
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 °C)
LogP
0.00940
Safety Information
Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
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 |
