Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H22O |
| Molecular Weight | 158.2811 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCOCCCCC
InChI
InChIKey=AOPDRZXCEAKHHW-UHFFFAOYSA-N
InChI=1S/C10H22O/c1-3-5-7-9-11-10-8-6-4-2/h3-10H2,1-2H3
| Molecular Formula | C10H22O |
| Molecular Weight | 158.2811 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Role of organic solvents on Pa-hydroxynitrile lyase interfacial activity and stability. | 2001 Jul 5 |
|
| Development and validation of a liquid chromatography-tandem mass spectrometry assay for the simultaneous quantitation of prednisolone and dipyridamole in human plasma and its application in a pharmacokinetic study. | 2009 Jul 12 |
|
| Phase equilibria study of the binary systems (1-butyl-3-methylimidazolium thiocyanate ionic liquid + organic solvent or water). | 2009 May 7 |
|
| Top-hits for H1N1pdm Identified by Virtual Screening Using Ensemble-based Docking. | 2009 Sep 2 |
|
| Ultrafast intramolecular charge transfer with N-(4-cyanophenyl)carbazole. Evidence for a LE precursor and dual LE + ICT fluorescence. | 2010 Dec 9 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:29:16 GMT 2023
by
admin
on
Sat Dec 16 04:29:16 GMT 2023
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| Record UNII |
4G19C1NH3E
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| Record Status |
Validated (UNII)
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| Record Version |
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4G19C1NH3E
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