Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H8N2 |
| Molecular Weight | 108.1411 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(N)N=CC=C1
InChI
InChIKey=RGDQRXPEZUNWHX-UHFFFAOYSA-N
InChI=1S/C6H8N2/c1-5-3-2-4-8-6(5)7/h2-4H,1H3,(H2,7,8)
| Molecular Formula | C6H8N2 |
| Molecular Weight | 108.1411 |
| 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, crystal structure, quantum chemical calculations, DNA interactions, and antimicrobial activity of [Ag(2-amino-3-methylpyridine)(2)]NO(3) and [Ag(pyridine-2-carboxaldoxime)NO(3)]. | 2010-11-01 |
|
| Bis(2-amino-3-methyl-pyridine)-dichlorido-cobalt(II). | 2010-09-25 |
|
| 2-Amino-3-methyl-pyridinium 2-amino-5-methyl-pyridinium sulfate monohydrate. | 2009-11-21 |
|
| 2-Methyl-N-[(3-methyl-2-pyrid-yl)carbamothio-yl]benzamide. | 2008-04-10 |
|
| Metal-organic cooperative catalysis in C-H and C-C bond activation and its concurrent recovery. | 2008-02 |
|
| Combining nucleoside analogues to achieve recognition of oligopurine tracts by triplex-forming oligonucleotides at physiological pH. | 2005-12-05 |
|
| Chelation-assisted carbon-hydrogen and carbon-carbon bond activation by transition metal catalysts. | 2002-06-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:48:57 GMT 2025
by
admin
on
Mon Mar 31 18:48:57 GMT 2025
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| Record UNII |
Y2WWD85QY6
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| Record Status |
Validated (UNII)
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