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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

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis, evaluation and QSAR studies of highly potent aromatase inhibitors of the piperidinedione type.
2001 Feb
Thermal activation of hydrocarbon C-H bonds by tungsten alkylidene complexes.
2001 Jan 31
Synthesis and calcium channel antagonist activity of new 1,4-dihydropyridine derivatives containing dichloroimidazolyl substituents.
2002
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 Dec 18
Fabrication of 3-dimensional PbZr(1-x)Ti(x)O3 nanoscale thin film capacitors for high density ferroelectric random access memory devices.
2006 Nov
Synthesis of carbon-11 labeled sulfonanilide analogues as new potential PET agents for imaging of aromatase in breast cancer.
2007 Jan 15
Dynamics of glass-forming liquids. XII. Dielectric study of primary and secondary relaxations in ethylcyclohexane.
2008 Mar 28
Effect of cycloalkyl glycosides of muramyl dipeptide on antibacterial resistance of mice and cytokine production by human mononuclear cells.
2009 Oct
Synthesis and SAR of thiazolidinedione derivatives as 15-PGDH inhibitors.
2010 Feb 15
Simple in situ monitoring of a complex catalytic reaction network at high pressure by attenuated total reflection Fourier transform infrared spectroscopy.
2010 Mar
Activation energy of the two-proton phototautomerism in 7-azaindole dimer and its medium-dependence.
2010 May 13
Name Type Language
ETHYLCYCLOHEXANE
Systematic Name English
SWACLEAN ECH
Brand 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 Fri Dec 15 19:42:48 GMT 2023 , Edited by admin on Fri Dec 15 19:42:48 GMT 2023
PRIMARY
CAS
1678-91-7
Created by admin on Fri Dec 15 19:42:48 GMT 2023 , Edited by admin on Fri Dec 15 19:42:48 GMT 2023
PRIMARY
ECHA (EC/EINECS)
216-835-0
Created by admin on Fri Dec 15 19:42:48 GMT 2023 , Edited by admin on Fri Dec 15 19:42:48 GMT 2023
PRIMARY
FDA UNII
567IJI1215
Created by admin on Fri Dec 15 19:42:48 GMT 2023 , Edited by admin on Fri Dec 15 19:42:48 GMT 2023
PRIMARY
NSC
8880
Created by admin on Fri Dec 15 19:42:48 GMT 2023 , Edited by admin on Fri Dec 15 19:42:48 GMT 2023
PRIMARY
PUBCHEM
15504
Created by admin on Fri Dec 15 19:42:48 GMT 2023 , Edited by admin on Fri Dec 15 19:42:48 GMT 2023
PRIMARY