4-Biphenylboronic acid

Product Information

Molecular Formula:
C12H11O2B
Molecular Weight:
198.03
Description
4-Biphenylboronic acid is a highly versatile compound that holds immense significance within the biomedical sector as a pivotal pharmaceutical intermediate. Its indispensability lies in aiding the synthesis of an array of drugs intended to combat an extensive range of ailments, including cancer, diabetes, and inflammation.
Synonyms
RARECHEM AH PB 0261; (1,1'-BIPHENYL-4-YL)BORONIC ACID; AKOS BRN-0030; 4-PHENYLBENZENEBORONIC ACID; 4-PHENYLPHENYLBORONIC ACID; 4-BIPHENYLBORONIC ACID
IUPAC Name
(4-phenylphenyl)boronic acid
Canonical SMILES
B(C1=CC=C(C=C1)C2=CC=CC=C2)(O)O
InChI
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
Boiling Point
385.5ºC at 760 mmHg
Melting Point
232-245ºC
Flash Point
Not applicable
Purity
98%
Density
1.18 g/cm3
Appearance
White to off-white solid

Computed Properties

Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
2
Exact Mass
198.0852098 g/mol
Monoisotopic Mass
198.0852098 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
182
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113968824-A 2,3, 5-trisubstituted pyrazine compound and preparation method and application thereof 2021-11-29
CN-114031623-A C14Amino-substituted tetrandrine derivative and preparation and application thereof 2021-11-12
CN-114057606-A Organic luminescent material containing terphenyl, preparation method and application 2021-11-11
CN-113880714-A Synthesis method of carbonyl alpha-position monomethyl substituted compound 2021-09-30
CN-113880854-A Organic compound containing spiro furocarbazole structure and application thereof 2021-09-30
CN-113816909-A Organic electroluminescent material containing phenanthrene structure and device thereof 2021-09-15
CN-113731504-A Catalyst and preparation method and application thereof 2021-09-09
CN-113930790-A Synthetic method of aryl selenide compound 2021-09-07
CN-113620901-A Crown ether derived chiral 1,1 '-bi-2, 2' -naphthol, preparation method and application thereof 2021-08-31
CN-113563590-A Novel high-temperature-resistant boron-silicon resin and synthetic method thereof 2021-08-09

Literatures

PMID Publication Date Title Journal
21580588 2010-03-03 2-Bromo-p-terphen-yl Acta crystallographica. Section E, Structure reports online
19731939 2009-10-08 Synthesis and evaluation of 3-(dihydroxyboryl)benzoic acids as D,D-carboxypeptidase R39 inhibitors Journal of medicinal chemistry
18983140 2008-11-27 Discovery of boronic acids as novel and potent inhibitors of fatty acid amide hydrolase Journal of medicinal chemistry
17297238 2007-02-01 Enhancing effect of phenylboronic acid compounds and their interactions with the diol groups of saccharides in a capillary electrophoresis-chemiluminescence detection system Analytical sciences : the international journal of the Japan Society for Analytical Chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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