Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H7N |
| Molecular Weight | 81.1158 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=CN1
InChI
InChIKey=TVCXVUHHCUYLGX-UHFFFAOYSA-N
InChI=1S/C5H7N/c1-5-3-2-4-6-5/h2-4,6H,1H3
| Molecular Formula | C5H7N |
| Molecular Weight | 81.1158 |
| 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 |
|---|---|---|
| (1H-Pyrrol-2-ylmethylidene)(3-{[(1H-pyrrol-2-ylmethylidene)amino]methyl}benzyl)amine. | 2010-11-17 |
|
| Regioselective formation of alpha-vinylpyrroles from the ruthenium-catalyzed coupling reaction of pyrroles and terminal alkynes involving C-H bond activation. | 2010-05-07 |
|
| Two new tropane alkaloids from the bark of Erythroxylum vacciniifolium Mart. (Erythroxylaceae). | 2009-10 |
|
| Metabolism of 5-isopropyl-6-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(2-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine (BMS-645737): identification of an unusual N-acetylglucosamine conjugate in the cynomolgus monkey. | 2008-12 |
|
| Alkyl peroxides reveal the ring opening mechanism of verdoheme catalyzed by heme oxygenase. | 2008-04-02 |
|
| Methylpyrrole tropane alkaloids from the bark of Erythroxylum vacciniifolium. | 2005-08 |
|
| Electronic structures of five-coordinate iron(III) porphyrin complexes with highly ruffled porphyrin ring. | 2004-08-09 |
|
| Importance of the C-H...N weak hydrogen bonding on the coordination structures of manganese(III) porphyrin complexes. | 2003-04-07 |
|
| Retinoic acid metabolism inhibition by 3-azolylmethyl-1H-indoles and 2, 3 or 5-(alpha-azolylbenzyl)-1H-indoles. | 2003-04 |
|
| Minor groove DNA binders as antimicrobial agents. 1. Pyrrole tetraamides are potent antibacterials against vancomycin resistant Enterococci [corrected] and methicillin resistant Staphylococcus aureus. | 2002-02-14 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:48:41 GMT 2025
by
admin
on
Mon Mar 31 19:48:41 GMT 2025
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| Record UNII |
486RY4814O
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| Record Status |
Validated (UNII)
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| Record Version |
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