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Merck
모든 사진(2)

주요 문서

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523968

Sigma-Aldrich

3-Hydroxyphenylboronic acid

≥95.0%

동의어(들):

3-Hydroxybenzeneboronic acid, m-Hydroxybenzeneboronic acid

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모든 사진(2)

About This Item

Linear Formula:
HOC6H4B(OH)2
CAS Number:
87199-18-6
Molecular Weight:
137.93
MDL number:
MFCD01074603
UNSPSC 코드:
12352103
PubChem Substance ID:
24874382
NACRES:
NA.22

Quality Level

100

분석

≥95.0%

mp

210-213 °C (dec.) (lit.)

SMILES string

OB(O)c1cccc(O)c1

InChI

1S/C6H7BO3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8-10H

InChI key

WFWQWTPAPNEOFE-UHFFFAOYSA-N

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애플리케이션

3-Hydroxyphenylboronic acid (3-HPBA) can be used as a reagent:
  • In Suzuki-Miyaura coupling reactions with aryl halides for the formation of C-C bond in the presence of Pd catalyst.
  •  To synthesize boron/nitrogen-doped polymer nano/microspheres by hydrothermal polymerization with formaldehyde and ammonia.      
  • To prepare carbon quantum dots based on 3-HPBA as selective fructose sensor.     
  • In the development of modified electrodes for electrochemical biosensors.

각주

Contains varying amounts of anhydride

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

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시험 성적서(COA)

Lot/Batch Number
SHBR7147
03006AI
17606LO
12521EO
09811LO

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문서 라이브러리 방문

Diana M A Crista et al.
Journal of fluorescence, 29(1), 265-270 (2019-01-07)
The selective fluorescence sensing of fructose was achieved by fluorescence quenching of the emission of hydrothermal-synthesized carbon quantum dots prepared by 3-hydroxyphenylboronic acid. Quantification of fructose was possible in aqueous solutions with pH of 9 (Limit of Detection LOD and
Facile synthesis of monodisperse bulk boron-and nitrogen-doped carbon nano/microspheres
Zhao J, et al.
Journal of Material Chemistry A, 6(46), 23780-23786 (2018)
Synthesis of hyperbranched polythiophene with a controlled degree of branching via catalyst-transfer Suzuki-Miyaura coupling reaction
Segawa Y, et al.
Polym. Chem., 4(4), 1208-1215 (2013)
Recent progress in electrochemical biosensors based on phenylboronic acid and derivatives
Anzai J-i
Materials Science and Engineering, C, 67, 737-746 (2016)
Mingyan Zhu et al.
ACS combinatorial science, 14(2), 124-134 (2011-12-21)
As a continuation of our previous report (J. Comb. Chem.2010, 12, 548-558), we accomplished the diversity-oriented synthesis of polyheterocyclic small-molecule library with privileged benzopyran substructure. To ensure the synthetic efficiency, we utilized the solid-phase parallel platform and the fluorous-tag-based solution-phase
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