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Sigma-Aldrich

4-Biphenylborsäure

≥95.0%

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About This Item

Lineare Formel:
C6H5C6H4B(OH)2
CAS-Nummer:
5122-94-1
Molekulargewicht:
198.03
MDL-Nummer:
MFCD00093311
UNSPSC-Code:
12352103
PubChem Substanz-ID:
24871894
NACRES:
NA.22

Assay

≥95.0%

mp (Schmelzpunkt)

232-245 °C (lit.)

SMILES String

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

InChIKey

XPEIJWZLPWNNOK-UHFFFAOYSA-N

Verwandte Kategorien

Sonstige Hinweise

Contains varying amounts of anhydride

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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4-(N-Boc-amino)phenylborsäure ≥95.0%

Sigma-Aldrich

565814

4-(N-Boc-amino)phenylborsäure

Phenylboronsäure 95%

Sigma-Aldrich

P20009

Phenylboronsäure

4-Jodbiphenyl 97%

Sigma-Aldrich

637769

4-Jodbiphenyl

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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
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
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
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