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 |
---|---|---|
Retinoic acid metabolism inhibition by 3-azolylmethyl-1H-indoles and 2, 3 or 5-(alpha-azolylbenzyl)-1H-indoles. | 2003 Apr |
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Importance of the C-H...N weak hydrogen bonding on the coordination structures of manganese(III) porphyrin complexes. | 2003 Apr 7 |
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Electronic structures of five-coordinate iron(III) porphyrin complexes with highly ruffled porphyrin ring. | 2004 Aug 9 |
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Methylpyrrole tropane alkaloids from the bark of Erythroxylum vacciniifolium. | 2005 Aug |
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Alkyl peroxides reveal the ring opening mechanism of verdoheme catalyzed by heme oxygenase. | 2008 Apr 2 |
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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 Dec |
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Two new tropane alkaloids from the bark of Erythroxylum vacciniifolium Mart. (Erythroxylaceae). | 2009 Oct |
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Regioselective formation of alpha-vinylpyrroles from the ruthenium-catalyzed coupling reaction of pyrroles and terminal alkynes involving C-H bond activation. | 2010 May 7 |
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(1H-Pyrrol-2-ylmethylidene)(3-{[(1H-pyrrol-2-ylmethylidene)amino]methyl}benzyl)amine. | 2010 Nov 17 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:34:49 GMT 2023
by
admin
on
Fri Dec 15 19:34:49 GMT 2023
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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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