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Details

Stereochemistry ACHIRAL
Molecular Formula C6H12
Molecular Weight 84.1595
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHYLCYCLOPENTANE

SMILES

CC1CCCC1

InChI

InChIKey=GDOPTJXRTPNYNR-UHFFFAOYSA-N
InChI=1S/C6H12/c1-6-4-2-3-5-6/h6H,2-5H2,1H3

HIDE SMILES / InChI

Molecular Formula C6H12
Molecular Weight 84.1595
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A three year study on 14 VOCs at one site in Rome: levels, seasonal variations, indoor/outdoor ratio and temporal trends.
2010-10
Effects of gasoline components on MTBE and TBA cometabolism by Mycobacterium austroafricanum JOB5.
2010-07
Development and validation of a headspace gas chromatographic method for the determination of residual solvents in arterolane (RBx11160) maleate bulk drug.
2010-01
Approach to estimation of absorption of aliphatic hydrocarbons diffusing from interior materials in an automobile cabin by inhalation toxicokinetic analysis in rats.
2010-01
Rate constants of nine C6-C9 alkanes with OH from 230 to 379 K: chemical tracers for [OH].
2009-04-30
Source apportionment of human personal exposure to volatile organic compounds in homes, offices and outdoors by chemical mass balance and genetic algorithm receptor models.
2008-12-15
Substituent effects on the rearrangements of cyclohexyl to cyclopentyl radicals involving avermectin-related radicals.
2008-11-07
First synthesis and anti-HIV evaluation of 4'-methyl-cyclopentanyl 9-deazaadenosine.
2008-10
Rearrangement of a cyclohexyl radical to a cyclopentylmethyl radical on the avermectin skeleton.
2008-06-05
Gas chromatographic analysis of petroleum associated condensate oil with simultaneous determination of some characteristic physical parameters.
2008-05-22
Release of MCP-1 and IL-8 from lung epithelial cells exposed to volatile organic compounds.
2008-03
An ab initio and density functional theory study of radical-clock reactions.
2008-02-15
Measurements of the 12C/13C kinetic isotope effects in the gas-phase reactions of light alkanes with chlorine atoms.
2007-01-25
Effects of molecular size and structure on self-diffusion coefficient and viscosity for saturated hydrocarbons having six carbon atoms.
2007
Structure-activity relationships of 1,5-biaryl pyrroles as EP1 receptor antagonists.
2006-07-15
Thermal chemistry of 1-methyl-1-cyclopentene and methylene cyclopentane on Pt(111) surfaces: evidence for double-bond isomerization.
2006-05-18
Mechanistic investigations of the ethylene tetramerisation reaction.
2005-08-03
The crystal structures of semi-synthetic aequorins.
2005-02
Benzene formation during aquasonolysis of selected cyclic C6Hx hydrocarbons.
2005-01
Hydrosilylation of dienes by yttrium hydrido complexes containing a linked amido-cyclopentadienyl ligand.
2004-08-07
Mechanism of palladium-catalyzed diene cyclization/hydrosilylation: direct observation of intramolecular carbometalation.
2004-05-26
Aquasonolysis of selected cyclic C(6)H(x) hydrocarbons.
2004-05
Conformational restriction of methionyl tRNA synthetase inhibitors leading to analogues with potent inhibition and excellent gram-positive antibacterial activity.
2003-04-07
Does metal ion complexation make radical clocks run fast?
2003-03-05
Dietary conjugated linoleic acid with fish oil alters yolk n-3 and trans fatty acid content and volatile compounds in raw, cooked, and irradiated eggs.
2002-10
Rearrangement of annelated housanes to triquinane-like hydrocarbons by electron transfer (1,3-cyclopentanediyl radical cations) and acid catalysis (cyclopentyl carbenium ions).
2002-01-25
The influence of maternal exposure to volatile organic compounds on the cytokine secretion profile of neonatal T cells.
2002
Ultrafast dynamics of cyclohexene and cyclohexene-d10 excited at 200 nm.
2001-07-25
Synthesis, evaluation and QSAR studies of highly potent aromatase inhibitors of the piperidinedione type.
2001-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:11:32 GMT 2025
Edited
by admin
on Mon Mar 31 21:11:32 GMT 2025
Record UNII
5G26CC1ASK
Record Status Validated (UNII)
Record Version
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Name Type Language
NSC-24836
Preferred Name English
METHYLCYCLOPENTANE
Systematic Name English
METHYL CYCLOPENTANE
Systematic Name English
Code System Code Type Description
NSC
24836
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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CAS
96-37-7
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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ECHA (EC/EINECS)
202-503-2
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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WIKIPEDIA
METHYLCYCLOPENTANE
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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HSDB
876
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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CHEBI
88429
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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EPA CompTox
DTXSID3025590
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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PUBCHEM
7296
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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FDA UNII
5G26CC1ASK
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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