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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
Structure of 2-METHYLPYRROLE

SMILES

CC1=CC=CN1

InChI

InChIKey=TVCXVUHHCUYLGX-UHFFFAOYSA-N
InChI=1S/C5H7N/c1-5-3-2-4-6-5/h2-4,6H,1H3

HIDE SMILES / InChI

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

PubMed

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

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 19:34:49 GMT 2023
Edited
by admin
on Fri Dec 15 19:34:49 GMT 2023
Record UNII
486RY4814O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-METHYLPYRROLE
Systematic Name English
NSC-81346
Code English
2-METHYL-1H-PYRROLE
Systematic Name English
Code System Code Type Description
NSC
81346
Created by admin on Fri Dec 15 19:34:49 GMT 2023 , Edited by admin on Fri Dec 15 19:34:49 GMT 2023
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FDA UNII
486RY4814O
Created by admin on Fri Dec 15 19:34:49 GMT 2023 , Edited by admin on Fri Dec 15 19:34:49 GMT 2023
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PUBCHEM
12489
Created by admin on Fri Dec 15 19:34:49 GMT 2023 , Edited by admin on Fri Dec 15 19:34:49 GMT 2023
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CAS
636-41-9
Created by admin on Fri Dec 15 19:34:49 GMT 2023 , Edited by admin on Fri Dec 15 19:34:49 GMT 2023
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ECHA (EC/EINECS)
211-255-4
Created by admin on Fri Dec 15 19:34:49 GMT 2023 , Edited by admin on Fri Dec 15 19:34:49 GMT 2023
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EPA CompTox
DTXSID70212976
Created by admin on Fri Dec 15 19:34:49 GMT 2023 , Edited by admin on Fri Dec 15 19:34:49 GMT 2023
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