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90770-88-0 | 4,4'-DIHYDROXY-2,2'-BIPYRIDINE
CAS No: 90770-88-0 Catalog No: AG00GYG5 MDL No:MFCD08704189
Product Description
Catalog Number:
AG00GYG5
Chemical Name:
4,4'-DIHYDROXY-2,2'-BIPYRIDINE
CAS Number:
90770-88-0
MDL Number:
MFCD08704189
IUPAC Name:
2-(4-oxo-1H-pyridin-2-yl)-1H-pyridin-4-one
InChI:
InChI=1S/C10H8N2O2/c13-7-1-3-11-9(5-7)10-6-8(14)2-4-12-10/h1-6H,(H,11,13)(H,12,14)
InChI Key:
JHDFNETXVFHWEE-UHFFFAOYSA-N
Properties
Complexity:
374
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
188.059g/mol
Formal Charge:
0
Heavy Atom Count:
14
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
188.186g/mol
Monoisotopic Mass:
188.059g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
58.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0
Literature
| Title | Journal |
|---|---|
| Structural, electronic and acid/base properties of [Ru(bpy(OH)2)3]2+ (bpy(OH)2 = 4,4'-dihydroxy-2,2'-bipyridine). | Dalton transactions (Cambridge, England : 2003) 20121028 |
| Highly efficient D2 generation by dehydrogenation of formic acid in D2O through H+/D+ exchange on an iridium catalyst: application to the synthesis of deuterated compounds by transfer deuterogenation. | Chemistry (Weinheim an der Bergstrasse, Germany) 20120723 |
| Interconversion between formic acid and H(2)/CO(2) using rhodium and ruthenium catalysts for CO(2) fixation and H(2) storage. | ChemSusChem 20110418 |
| Structural, electronic, and acid/base properties of [Ru(bpy)2(bpy(OH)2)]2+ (bpy = 2,2'-bipyridine, bpy(OH)2 = 4,4'-dihydroxy-2,2'-bipyridine). | Inorganic chemistry 20110404 |
| pH-Dependent catalytic activity and chemoselectivity in transfer hydrogenation catalyzed by iridium complex with 4,4'-dihydroxy-2,2'-bipyridine. | Chemistry (Weinheim an der Bergstrasse, Germany) 20080101 |
| Synthesis of novel dendritic 2,2'-bipyridine ligands and their application to Lewis acid-catalyzed diels-alder and three-component condensation reactions. | The Journal of organic chemistry 20071012 |
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