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4589-12-2 | N-(pyridin-2-yl)benzamide
CAS No: 4589-12-2 Catalog No: AG01C3LK MDL No:MFCD00459601
Product Description
Catalog Number:
AG01C3LK
Chemical Name:
N-(pyridin-2-yl)benzamide
CAS Number:
4589-12-2
Molecular Formula:
C12H10N2O
Molecular Weight:
198.2206
MDL Number:
MFCD00459601
IUPAC Name:
N-pyridin-2-ylbenzamide
InChI:
InChI=1S/C12H10N2O/c15-12(10-6-2-1-3-7-10)14-11-8-4-5-9-13-11/h1-9H,(H,13,14,15)
InChI Key:
LZIJKEIPCFEOLH-UHFFFAOYSA-N
SMILES:
O=C(c1ccccc1)Nc1ccccn1
NSC Number:
2011
Properties
Complexity:
212
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
198.079g/mol
Formal Charge:
0
Heavy Atom Count:
15
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
198.225g/mol
Monoisotopic Mass:
198.079g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
42A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.3
Literature
| Title | Journal |
|---|---|
| Small-molecule inhibitor leads of ribosome-inactivating proteins developed using the doorstop approach. | PloS one 20110101 |
| False positives in a reporter gene assay: identification and synthesis of substituted N-pyridin-2-ylbenzamides as competitive inhibitors of firefly luciferase. | Journal of medicinal chemistry 20080814 |
| Hydrogen bond-free flavin redox properties: managing flavins in extreme aprotic solvents. | Organic & biomolecular chemistry 20080621 |
| Heterocyclic analogues of N-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butyl)arylcarboxamides with functionalized linking chains as novel dopamine D3 receptor ligands: potential substance abuse therapeutic agents. | Journal of medicinal chemistry 20070823 |
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. | Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501 |
| Heavier alkali metal complexes of 2-phenylamidopyridine: an X-ray crystallographic and theoretical study of a structurally diverse series of crown ether adducts. | Dalton transactions (Cambridge, England : 2003) 20040821 |
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