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3-Vinylphenylboronic acid_Molecular_structure_CAS_15016-43-0)
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3-Vinylphenylboronic acid

Catalog No. 680575 Name Sigma Aldrich
CAS Number 15016-43-0 Website http://www.sigmaaldrich.com
M. F. C8H9BO2 Telephone 1-800-521-8956
M. W. 147.96686 Fax
Purity Email
Storage Chembase ID: 91518

SYNONYMS

Title
3-乙烯基苯硼酸
IUPAC name
(3-ethenylphenyl)boronic acid
IUPAC Traditional name
3-ethenylphenylboronic acid
Synonyms
m-Vinylbenzeneboronic acid
(3-Ethenylphenyl)boronic acid

DATABASE IDS

CAS Number 15016-43-0
MDL Number MFCD01074679
PubChem SID 24885576

PROPERTIES

Empirical Formula (Hill Notation) C8H9BO2
Melting Point 141-147 °C
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS Precautionary statements P301 + P310
RID/ADR UN 2811 6.1/PG 3
Risk Statements 22
Storage Temperature 2-8°C
Hazard Class 6.1
UN Number 2811
Packing Group 3
German water hazard class 3

DETAILS

Description (简体中文)
General description
可能含不定量的酸酐。
包装
1, 10 g in glass bottle
Application
Reactant involved in:
• Suzuki-Miyaura reactions1
• Molecular imprinting of fructose and pinacol2
• Synthesis of arylmercapturic acids via Chen-Lam-Evans arylation3
• Three-component cross-coupling yeilding diarylketones4
• Generation of acyl anion equivalents5
Description (English)
General description
May contain varying amounts of anhydride.
Packaging
1, 10 g in glass bottle
Application
Reactant involved in:
• Suzuki-Miyaura reactions1
• Molecular imprinting of fructose and pinacol2
• Synthesis of arylmercapturic acids via Chen-Lam-Evans arylation3
• Three-component cross-coupling yeilding diarylketones4
• Generation of acyl anion equivalents5

REFERENCES