2-Bromopyridine-3-boronic acid pinacol ester

Product Information

Molecular Formula:
C11H15BBrNO2
Molecular Weight:
283.96
Description
2-Bromopyridine-3-boronic acid pinacol ester is utilized in bio-medical research, widely applied in the synthesis of various pharmaceutical compounds. Specifically, it plays an essential role in drug discovery processes aiming at cardiovascular diseases and cancer treatment.
Synonyms
2-BROMO-3-PYRIDINEBORONIC ACID PINACOL ESTER; 2-BROMO-3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDINE; 2-BROMOPYRIDINE-3-BORONIC ACID PINACOL ESTER; 2-Bromopyridine-3-boronic acid pinacol ester, Technical, 90%; REF DUPL: 2-Bromopyridine-3-boronic a
IUPAC Name
2-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Canonical SMILES
B1(OC(C(O1)(C)C)(C)C)C2=C(N=CC=C2)Br
InChI
InChI=1S/C11H15BBrNO2/c1-10(2)11(3,4)16-12(15-10)8-6-5-7-14-9(8)13/h5-7H,1-4H3
InChI Key
QAQDSIBZRCSYAR-UHFFFAOYSA-N
Boiling Point
353.9°C at 760mmHg
Flash Point
>230 °F
Purity
95%
Density
1.329
Appearance
Colorless to yellow liquid

Safety Information

Hazards
H315-H319-H335
Precautionary Statement
P261-P305 + P351 + P338

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
1
Exact Mass
283.03792 g/mol
Monoisotopic Mass
283.03792 g/mol
Topological Polar Surface Area
31.4Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
257
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-111435705-A Repairing agent and repairing method thereof and method for preparing photoelectric film 2019-06-12
CN-112086564-A Passivating agent and passivation method thereof and method for preparing semiconductor film 2019-06-12
WO-2020248864-A1 Passivator, passivation method therefor and method for preparing semiconductor film 2019-06-12
TW-202003734-A Resin composition, laminate, semiconductor wafer with resin composition layer, mounting substrate for semiconductor with resin composition layer, and semiconductor device 2018-04-26
WO-2019208614-A1 Resin composition, laminate, resin composition layer-attached semiconductor wafer, substrate for mounting resin composition layer-attached semiconductor, and semiconductor device 2018-04-26
EP-3786200-A1 Resin composition, laminate, resin composition layer-attached semiconductor wafer, substrate for mounting resin composition layer-attached semiconductor, and semiconductor device 2018-04-26
KR-20210004971-A Resin composition, laminate, semiconductor wafer with resin composition layer, semiconductor mounting substrate with resin composition layer, and semiconductor device 2018-04-26
US-2021277221-A1 Resin composition, laminate, semiconductor wafer with resin composition layer, substrate for mounting semiconductor with resin composition layer and semiconductor device 2018-04-26
JP-2014169285-A Pharmaceuticals consisting of uracil derivatives 2013-02-05
JP-5799117-B2 Pharmaceuticals consisting of uracil derivatives 2013-02-05
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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