Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H8N2 |
| Molecular Weight | 156.1839 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1=CN=C(C=C1)C2=CC=NC=C2
InChI
InChIKey=RMHQDKYZXJVCME-UHFFFAOYSA-N
InChI=1S/C10H8N2/c1-2-6-12-10(3-1)9-4-7-11-8-5-9/h1-8H
| Molecular Formula | C10H8N2 |
| Molecular Weight | 156.1839 |
| 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 |
|---|---|---|
| Synthesis and characterization of alkali-metal salts of 2,2'- and 2,4'-bipyridyl radicals and dianions. | 2009-09-07 |
|
| Polymeric networks of copper(II) phenylmalonate with heteroaromatic n-donor ligands: synthesis, crystal structure, and magnetic properties. | 2005-10-31 |
|
| Antimicrobial activity of a series of 1-alkyl-2-(4-pyridyl)pyridinium bromides against Gram-Positive and Gram-Negative bacteria. | 2005-01-09 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:00:53 GMT 2025
by
admin
on
Mon Mar 31 19:00:53 GMT 2025
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| Record UNII |
C6SN6RU851
|
| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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209-467-7
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C6SN6RU851
Created by
admin on Mon Mar 31 19:00:53 GMT 2025 , Edited by admin on Mon Mar 31 19:00:53 GMT 2025
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