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
SMILES
CCC1CCCCC1
InChI
InChIKey=IIEWJVIFRVWJOD-UHFFFAOYSA-N
InChI=1S/C8H16/c1-2-8-6-4-3-5-7-8/h8H,2-7H2,1H3
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
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 | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 |
SUBSTANCE RECORD