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483451

Sigma-Aldrich

4-Biphenylboronic acid

≥95.0%

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R$ 669,00
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5 G
R$ 669,00
25 G
R$ 913,00

About This Item

Fórmula linear:
C6H5C6H4B(OH)2
Número CAS:
Peso molecular:
198.03
Número MDL:
Código UNSPSC:
12352103
ID de substância PubChem:
NACRES:
NA.22

R$ 669,00


Check Cart for Availability

Solicite uma grande encomenda

Nível de qualidade

Ensaio

≥95.0%

pf

232-245 °C (lit.)

grupo funcional

phenyl

cadeia de caracteres SMILES

OB(O)c1ccc(cc1)-c2ccccc2

InChI

1S/C12H11BO2/c14-13(15)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,14-15H

chave InChI

XPEIJWZLPWNNOK-UHFFFAOYSA-N

Outras notas

Contains varying amounts of anhydride

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Kazuhiko Tsukagoshi et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 23(2), 227-230 (2007-02-14)
In our previous study, we proposed molecular recognition of mono- and disaccharides making use of the interaction between their diol groups and p-iodophenylboronic acid in capillary electrophoresis with a chemiluminescence detection system. Here, to extend our knowledge of molecular recognition
L J Kricka et al.
Journal of bioluminescence and chemiluminescence, 11(3), 137-147 (1996-05-01)
The enhancers 1,1'-biphenyl-4-yl boronic acid and 4-iodophenol act synergistically in the horseradish peroxidase-catalysed oxidation of luminol. This concentration-dependent effect reduces background, increases signal and hence improves signal/background for detection of peroxidase. The same type of synergistic effect was found when
Steven R Inglis et al.
Journal of medicinal chemistry, 52(19), 6097-6106 (2009-09-08)
Penicillin binding proteins (PBPs) catalyze steps in the biosynthesis of bacterial cell walls and are the targets for the beta-lactam antibiotics. Non-beta-lactam based antibiotics that target PBPs are of interest because bacteria have evolved resistance to the beta-lactam antibiotics. Boronic
Anna Minkkilä et al.
Journal of medicinal chemistry, 51(22), 7057-7060 (2008-11-06)
A series of commercial phenyl-, heteroaryl-, alkyl-, and alkenylboronic acids were evaluated for their FAAH and MGL inhibitory activities. The compounds were generally selective for FAAH, with IC50 in the nanomolar or low-micromolar range. Eight of these compounds inhibited MGL
Fugui Zhu et al.
The Plant cell, 32(9), 2855-2877 (2020-09-06)
Because of the large amount of energy consumed during symbiotic nitrogen fixation, legumes must balance growth and symbiotic nodulation. Both lateral roots and nodules form on the root system, and the developmental coordination of these organs under conditions of reduced

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