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Home > Boronic Acids > 163105-89-3
163105-89-3 | Boronic acid, B-(6-methoxy-3-pyridinyl)-
CAS No: 163105-89-3 Catalog No: AG001TR5 MDL No:MFCD02093044
Product Description
Catalog Number:
AG001TR5
Chemical Name:
Boronic acid, B-(6-methoxy-3-pyridinyl)-
CAS Number:
163105-89-3
Molecular Formula:
C6H8BNO3
Molecular Weight:
152.9436
MDL Number:
MFCD02093044
IUPAC Name:
(6-methoxypyridin-3-yl)boronic acid
InChI:
InChI=1S/C6H8BNO3/c1-11-6-3-2-5(4-8-6)7(9)10/h2-4,9-10H,1H3
InChI Key:
DHADXDMPEUWEAS-UHFFFAOYSA-N
SMILES:
COc1ccc(cn1)B(O)O
Properties
Complexity:
122
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
153.06g/mol
Formal Charge:
0
Heavy Atom Count:
11
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
152.944g/mol
Monoisotopic Mass:
153.06g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
62.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
| Title | Journal |
|---|---|
| Palladium-catalyzed cross-coupling reactions of pyridylboronic acids with heteroaryl halides bearing a primary amine group: synthesis of highly substituted bipyridines and pyrazinopyridines. | The Journal of organic chemistry 20050107 |
| 5-Pyrimidylboronic acid and 2-methoxy-5-pyrimidylboronic acid: new heteroarylpyrimidine derivatives via Suzuki cross-coupling reactions. | Organic & biomolecular chemistry 20040321 |
| Functionalized pyridylboronic acids and their Suzuki cross-coupling reactions to yield novel heteroarylpyridines. | The Journal of organic chemistry 20021018 |
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