2-VINYLPHENYLBORONIC ACID
Product Information
Molecular Formula
C8H9BO2
Molecular Weight
147.97
Description
2-Vinylphenylboronic acid, a compound extensively employed in the biomedical sector, showcases remarkable versatility. Owing to its distinctive configuration, it exhibits profound anti-inflammatory properties.
Synonyms
AKOS BRN-0141; 2-BORONOSTYRENE; 2-VINYLPHENYLBORONIC ACID; 2-VINYLBENZENEBORONIC ACID; RARECHEM AH PB 0210; styrene-2-boronic acid
IUPAC Name
(2-ethenylphenyl)boronic acid
SMILES
B(C1=CC=CC=C1C=C)(O)O
InChI
InChI=1S/C8H9BO2/c1-2-7-5-3-4-6-8(7)9(10)11/h2-6,10-11H,1H2
InChI Key
QHFAXRHEKNHTDH-UHFFFAOYSA-N
Boiling Point
313.7°C at 760mmHg
Melting Point
105-107°C
Flash Point
Not applicable
Purity
96%
Density
1.09g/cm3
Appearance
White crystalline powder
Safety Information
Hazards
H301 - H318
Precautionary Statement
P280 - P301 + P310 + P330 - P305 + P351 + P338 + P310
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
136
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-114045082-A | Composite coating with self-repairing, air-permeable and wear-resistant properties, and preparation method and application thereof | 2021-12-14 |
| 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 |
| WO-2022051583-A1 | Medium- or macro-cyclic benzyl-substituted heterocycle derivatives and their uses as orexin-2 receptor agonists | 2020-09-03 |
| CN-114075054-A | Dispersant for oil well cement and cement composition | 2020-08-14 |
| CN-111548714-A | Self-repairing water-based polymer composite coating agent and preparation method and application thereof | 2020-05-29 |
| WO-2021222353-A1 | Macrocyclic inhibitors of peptidylarginine deiminases | 2020-04-30 |
| WO-2021169963-A1 | Aromatic compound and use thereof in preparing antineoplastic drugs | 2020-02-24 |
| WO-2021158840-A1 | Macrocyclic pad4 inhibitors useful as immunosuppressant | 2020-02-06 |
| CN-110938074-A | Planar triphenylamine derivative with crosslinkable group and synthetic method thereof | 2019-11-10 |
| CN-111269365-A | Temperature-sensitive Wulff type boron affinity nano-particles and preparation method and application thereof | 2019-04-15 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 20685466 | 2010-06-30 | On-line coupling of in-tube boronate affinity solid phase microextraction with high performance liquid chromatography-electrospray ionization tandem mass spectrometry for the determination of cis-diol biomolecules | Talanta |
| 18482607 | 2008-06-02 | Selective adenosine-5'-monophosphate uptake by water-compatible molecularly imprinted polymer | Analytica chimica acta |
