483451
4-Biphenylboronic acid
≥95.0%
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About This Item
Fórmula lineal:
C6H5C6H4B(OH)2
Número de CAS:
Peso molecular:
198.03
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
assay
≥95.0%
mp
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
InChI key
XPEIJWZLPWNNOK-UHFFFAOYSA-N
Other Notes
Contains varying amounts of anhydride
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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
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
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A group of polyethers containing electroactive pendent 4,7-diarylfluorene chromophores have been prepared by the multi-step synthetic route. Full characterization of their structures has been presented. The polymeric materials represent derivatives of high thermal stability with initial thermal degradation temperatures in
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
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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