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680575

Sigma-Aldrich

3-Vinylphenylboronic acid

≥95%

Synonym(s):

(3-Ethenylphenyl)boronic acid, m-Vinylbenzeneboronic acid

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About This Item

Empirical Formula (Hill Notation):
C8H9BO2
CAS Number:
15016-43-0
Molecular Weight:
147.97
MDL number:
MFCD01074679
UNSPSC Code:
12352103
PubChem Substance ID:
24885576

Assay

≥95%

form

powder or crystals

mp

141-147 °C

storage temp.

2-8°C

SMILES string

OB(O)c1cccc(C=C)c1

InChI

1S/C8H9BO2/c1-2-7-4-3-5-8(6-7)9(10)11/h2-6,10-11H,1H2

InChI key

SYBQEKBVWDPVJM-UHFFFAOYSA-N

General description

May contain varying amounts of anhydride.

Application

Reactant involved in:
  • Suzuki-Miyaura reactions
  • Molecular imprinting of fructose and pinacol
  • Synthesis of arylmercapturic acids via Chen-Lam-Evans arylation
  • Three-component cross-coupling yeilding diarylketones
  • Generation of acyl anion equivalents

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301

Precautionary Statements

P301 + P310

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBC8957V
19096LMV
19096LM
08011AH

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Mengzhe Guo et al.
Journal of separation science, 39(17), 3428-3435 (2016-07-13)
Maltose, a common auxiliary material of pharmaceutical preparation, may disturb the analysis of total amino acids in sepia capsule by aldolization. Therefore, it is necessary to remove the maltose through a convenient method. In this work, a phenylboronic acid modified

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