Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H11N |
| Molecular Weight | 169.2224 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C(C1=CC=CC=C1)C2=NC=CC=C2
InChI
InChIKey=PCFUWBOSXMKGIP-UHFFFAOYSA-N
InChI=1S/C12H11N/c1-2-6-11(7-3-1)10-12-8-4-5-9-13-12/h1-9H,10H2
| Molecular Formula | C12H11N |
| Molecular Weight | 169.2224 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Ruthenium(II) complexes of 2-benzoylpyridine-derived thiosemicarbazones with cytotoxic activity against human tumor cell lines. | 2008-04 |
|
| Interaction between tetramethylcucurbit[6]uril and some pyridine derivates. | 2007-04-12 |
|
| Synthesis, characterization, and preliminary oxygenation studies of benzyl- and ethyl-substituted pyridine ligands of carboxylate-rich diiron(II) complexes. | 2006-01-23 |
|
| Oxidation of sulfide, phosphine, and benzyl substrates tethered to N-donor pyridine ligands in carboxylate-bridged diiron(II) complexes. | 2004-03-24 |
|
| Reactions of an amphoteric terminal tungsten methylidyne complex. | 2001-05-30 |
|
| Effect of 4-(4-chlorobenzyl)pyridine on rat hepatic microsomal cytochrome P450 and drug-metabolizing enzymes in vivo and in vitro. | 2001-05 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:48:38 GMT 2025
by
admin
on
Mon Mar 31 19:48:38 GMT 2025
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| Record UNII |
EW2N4V60MQ
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| Record Status |
Validated (UNII)
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| Record Version |
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7581
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202-979-1
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101-82-6
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DTXSID5059240
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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