Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H11N3 |
| Molecular Weight | 173.2144 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NN(C(N)=C1)C2=CC=CC=C2
InChI
InChIKey=FMKMKBLHMONXJM-UHFFFAOYSA-N
InChI=1S/C10H11N3/c1-8-7-10(11)13(12-8)9-5-3-2-4-6-9/h2-7H,11H2,1H3
| Molecular Formula | C10H11N3 |
| Molecular Weight | 173.2144 |
| 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 |
|---|---|---|
| One-pot combinatorial synthesis of 4-aryl-1H-thiopyrano[3,4-b]pyridine-5-one derivatives. | 2010-07-12 |
|
| 3,4,6-Trimethyl-1-phenyl-1H-pyrazolo-[3,4-b]pyridine. | 2010-07-10 |
|
| Ionic liquid-promoted multi-component reaction: novel and efficient preparation of pyrazolo[3,4-b]pyridinone, pyrazolo[3,4-b]-quinolinone and their hybrids with pyrimidine nucleoside. | 2010-02 |
|
| Diversity synthesis of pyrimido[4,5-b][1,6]naphthyridine and its derivatives under microwave irradiation. | 2009-08-22 |
|
| 4-(4-Bromo-phen-yl)-4,5,6,7-tetra-hydro-3-methyl-6-oxo-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile ethanol solvate. | 2008-09-13 |
|
| 6,7-Dihydro-4-(4-methoxy-phen-yl)-3-methyl-6-oxo-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile. | 2008-09-06 |
|
| 2-[(5-Amino-3-methyl-1-phenyl-1H-pyrazol-4-yl)(4-chloro-phen-yl)meth-yl]malononitrile. | 2008-04-26 |
|
| 6-Amino-3-methyl-4-(4-nitro-phen-yl)-1-phenyl-pyrazolo[3,4-b]pyridine-5-carbonitrile. | 2008-03-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:07:14 GMT 2025
by
admin
on
Mon Mar 31 21:07:14 GMT 2025
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| Record UNII |
X6087GEB2P
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| Record Status |
Validated (UNII)
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| Record Version |
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