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Details

Stereochemistry ACHIRAL
Molecular Formula C5H11N
Molecular Weight 85.1475
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-METHYLPYRROLIDINE

SMILES

CN1CCCC1

InChI

InChIKey=AVFZOVWCLRSYKC-UHFFFAOYSA-N
InChI=1S/C5H11N/c1-6-4-2-3-5-6/h2-5H2,1H3

HIDE SMILES / InChI

Molecular Formula C5H11N
Molecular Weight 85.1475
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
N-methylpiperidinemethyl, N-methylpyrrolidyl and N-methylpyrrolidinemethyl esters as PET radiotracers for acetylcholinesterase activity.
2003 Apr
Kinetics and mechanism of ring transformation of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium bromide to 2-methylimino-5-[2-(4-methoxyphenylamino)ethyl]thiazolidin-4-one.
2003 Apr 7
A new highly asymmetric chelation-controlled heck arylation.
2003 Mar 26
Physicochemical determinants for drug induced blockade of HERG potassium channels: effect of charge and charge shielding.
2003 Oct
N-n-alkylpyridinium analogs, a novel class of nicotinic receptor antagonists: selective inhibition of nicotine-evoked [3H] dopamine overflow from superfused rat striatal slices.
2003 Sep
A new class of potent non-imidazole H(3) antagonists: 2-aminoethylbenzofurans.
2004 Feb 9
Molecular dissection of tropisetron, an alpha7 nicotinic acetylcholine receptor-selective partial agonist.
2005 Apr 22
5-substituted, 6-substituted, and unsubstituted 3-heteroaromatic pyridine analogues of nicotine as selective inhibitors of cytochrome P-450 2A6.
2005 Jan 13
Synthesis of new, potent avermectin-like insecticidal agents.
2005 Jul 4
Direct synthesis of fused 1,2,3,4,5-pentathiepins.
2005 Oct 7
Abstracts of papers presented at the 2008 pittsburgh conference.
2008
1-Methyl-1-propyl-pyrrolidinium chloride.
2008 Feb 29
1,1'-Dimethyl-1,1'-(butane-1,4-di-yl)dipyrrolidinium dibromide methanol disolvate.
2008 Jan 11
5-(2-Pyrrolidinyl)oxazolidinones and 2-(2-pyrrolidinyl)benzodioxanes: synthesis of all the stereoisomers and alpha4beta2 nicotinic affinity.
2009 Feb 1
Using the cationic surfactants N-cetyl-N-methylpyrrolidinium bromide and 1-cetyl-3-methylimidazolium bromide for sweeping-micellar electrokinetic chromatography.
2009 Jul 3
Pyrrolidinium ionic liquid crystals with pendant mesogenic groups.
2009 May 19
Validation of capillary electrophoresis method for determination of N-methylpyrrolidine in cefepime for injection.
2010 Nov
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:47:24 GMT 2023
Edited
by admin
on Fri Dec 15 17:47:24 GMT 2023
Record UNII
06509TZU6C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-METHYLPYRROLIDINE
Systematic Name English
CEFEPIME IMPURITY G [EP IMPURITY]
Common Name English
PYRROLIDINE, 1-METHYL-
Systematic Name English
N-METHYLTETRAHYDROPYRROLE
Systematic Name English
NSC-65579
Code English
N-METHYLPYRROLIDINE
Systematic Name English
METHYLPYRROLIDINE, 1-
Systematic Name English
NSC-65
Code English
CEFEPIME DIHYDROCHLORIDE MONOHYDRATE IMPURITY G [EP IMPURITY]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
204-438-5
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID8042210
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
PUBCHEM
8454
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
NSC
65
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
CAS
120-94-5
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
FDA UNII
06509TZU6C
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
NSC
65579
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE INACTIVE
Converted rapidly to NMP-N-oxide
MINOR
URINE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP