483451
4-Biphenylboronic acid
≥95.0%
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About This Item
Linear Formula:
C6H5C6H4B(OH)2
CAS Number:
Molecular Weight:
198.03
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Quality Level
assay
≥95.0%
mp
232-245 °C (lit.)
functional group
phenyl
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
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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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 483451-25G | 04061832904849 |
| 483451-5G | 04061832904856 |