4-Vinylphenylboronic Acid - CAS 2156-04-9
Catalog: |
BB016962 |
Product Name: |
4-Vinylphenylboronic Acid |
CAS: |
2156-04-9 |
Synonyms: |
(4-ethenylphenyl)boronic acid; (4-ethenylphenyl)boronic acid |
IUPAC Name: | (4-ethenylphenyl)boronic acid |
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. |
Molecular Weight: | 147.97 |
Molecular Formula: | C8H9O2B |
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 °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) |
MDL: | MFCD00239441 |
LogP: | 0.00940 |
GHS Hazard Statement: | H302 (87.5%): Harmful if swallowed [Warning Acute toxicity, oral] |
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 |
Publication Number | Title | Priority Date |
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 | 20210708 |
CN-113354810-A | Clustering peptide with side chain containing functionalized biphenyl group and preparation method thereof | 20210607 |
CN-113214440-A | UCST type nonionic water-soluble polymer and preparation method and application thereof | 20210430 |
CN-113087721-A | Phenazine-containing nine-membered condensed ring crosslinkable micromolecule hole transport material and application thereof | 20210329 |
CN-113150205-A | Thermo-sensitive phenylboronic acid microgel for glycoprotein controlled release and signal amplification strategy and preparation method and application thereof | 20210322 |
PMID | Publication Date | Title | Journal |
22888741 | 20121001 | Synthesis and characterization of thermally and glucose-sensitive poly N-vinylcaprolactam-Based microgels | Journal of biomedical nanotechnology |
22967628 | 20120915 | Synthesis of water-compatible imprinted polymers of in situ produced fructosazine and 2,5-deoxyfructosazine | Talanta |
22762957 | 20120817 | 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 |
22707097 | 20120716 | Boronic Acid functionalized core-shell polymer nanoparticles prepared by distillation precipitation polymerization for glycopeptide enrichment | Chemistry (Weinheim an der Bergstrasse, Germany) |
22425210 | 20120713 | 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 |
Complexity: | 128 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 148.0695597 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 148.0695597 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 40.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Boronic Acids and Esters
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS