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Details

Stereochemistry ACHIRAL
Molecular Formula C8H16
Molecular Weight 112.2126
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYLCYCLOHEXANE

SMILES

CCC1CCCCC1

InChI

InChIKey=IIEWJVIFRVWJOD-UHFFFAOYSA-N
InChI=1S/C8H16/c1-2-8-6-4-3-5-7-8/h8H,2-7H2,1H3

HIDE SMILES / InChI

Molecular Formula C8H16
Molecular Weight 112.2126
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Activation energy of the two-proton phototautomerism in 7-azaindole dimer and its medium-dependence.
2010-05-13
Simple in situ monitoring of a complex catalytic reaction network at high pressure by attenuated total reflection Fourier transform infrared spectroscopy.
2010-03
Synthesis and SAR of thiazolidinedione derivatives as 15-PGDH inhibitors.
2010-02-15
Effect of cycloalkyl glycosides of muramyl dipeptide on antibacterial resistance of mice and cytokine production by human mononuclear cells.
2009-10
Dynamics of glass-forming liquids. XII. Dielectric study of primary and secondary relaxations in ethylcyclohexane.
2008-03-28
Multiple mechanical relaxations in ethylcyclohexane above the glass transition temperature.
2007-09-20
Effect of admicellar properties on adsolubilization: column studies and solute transport.
2007-03
Synthesis of carbon-11 labeled sulfonanilide analogues as new potential PET agents for imaging of aromatase in breast cancer.
2007-01-15
Origin of the pi-facial stereoselectivity in the addition of nucleophilic reagents to chiral aliphatic ketones as evidenced by high-level ab initio molecular-orbital calculations.
2006-12-18
Fabrication of 3-dimensional PbZr(1-x)Ti(x)O3 nanoscale thin film capacitors for high density ferroelectric random access memory devices.
2006-11
Investigation of bioactivation and toxicity of styrene in CYP2E1 transgenic cells.
2006-09-21
Thermodynamic study of alkyl-cyclohexanes in liquid, glassy, and crystalline states.
2006-08-07
Chiroptical properties of 2-chloropropionitrile.
2005-04-21
Synthesis and calcium channel antagonist activity of new 1,4-dihydropyridine derivatives containing dichloroimidazolyl substituents.
2002
Synthesis, evaluation and QSAR studies of highly potent aromatase inhibitors of the piperidinedione type.
2001-02
Thermal activation of hydrocarbon C-H bonds by tungsten alkylidene complexes.
2001-01-31
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:54:30 GMT 2025
Edited
by admin
on Mon Mar 31 19:54:30 GMT 2025
Record UNII
567IJI1215
Record Status Validated (UNII)
Record Version
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Name Type Language
SWACLEAN ECH
Preferred Name English
ETHYLCYCLOHEXANE
Systematic Name English
CYCLOHEXANE, ETHYL-
Systematic Name English
CYCLOHEXYLETHANE
Systematic Name English
1-ETHYL-CYCLOHEXANECARBALDEHYDE
Systematic Name English
NSC-8880
Code English
Code System Code Type Description
EPA CompTox
DTXSID1051779
Created by admin on Mon Mar 31 19:54:30 GMT 2025 , Edited by admin on Mon Mar 31 19:54:30 GMT 2025
PRIMARY
CAS
1678-91-7
Created by admin on Mon Mar 31 19:54:30 GMT 2025 , Edited by admin on Mon Mar 31 19:54:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
216-835-0
Created by admin on Mon Mar 31 19:54:30 GMT 2025 , Edited by admin on Mon Mar 31 19:54:30 GMT 2025
PRIMARY
FDA UNII
567IJI1215
Created by admin on Mon Mar 31 19:54:30 GMT 2025 , Edited by admin on Mon Mar 31 19:54:30 GMT 2025
PRIMARY
NSC
8880
Created by admin on Mon Mar 31 19:54:30 GMT 2025 , Edited by admin on Mon Mar 31 19:54:30 GMT 2025
PRIMARY
PUBCHEM
15504
Created by admin on Mon Mar 31 19:54:30 GMT 2025 , Edited by admin on Mon Mar 31 19:54:30 GMT 2025
PRIMARY