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 |
|
| Modification of calix[4]arenes with CMPO-functions at the wide rim. Synthesis, solution behavior, and separation of actinides from lanthanides. | 2003 Nov 21 |
|
| Short-term oral toxicity of pentyl ether, 1,4-diethoxybutane, and 1,6-dimethoxyhexane in male rats. | 2004 Jan |
|
| Immobilization of lipases on different carriers and their use in synthesis of pentyl isovalerates. | 2004 May |
|
| Simultaneous determination of three isomeric metabolites of tacrolimus (FK506) in human whole blood and plasma using high performance liquid chromatography-tandem mass spectrometry. | 2006 Jan 18 |
|
| Reduced sensitivity of influenza A (H5N1) to oseltamivir. | 2007 Sep |
|
| Ensemble-based virtual screening reveals potential novel antiviral compounds for avian influenza neuraminidase. | 2008 Jul 10 |
|
| 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
|
| Record UNII |
4G19C1NH3E
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
6571
Created by
admin on Sat Dec 16 04:29:16 GMT 2023 , Edited by admin on Sat Dec 16 04:29:16 GMT 2023
|
PRIMARY | |||
|
4G19C1NH3E
Created by
admin on Sat Dec 16 04:29:16 GMT 2023 , Edited by admin on Sat Dec 16 04:29:16 GMT 2023
|
PRIMARY | |||
|
m1872
Created by
admin on Sat Dec 16 04:29:16 GMT 2023 , Edited by admin on Sat Dec 16 04:29:16 GMT 2023
|
PRIMARY | Merck Index | ||
|
693-65-2
Created by
admin on Sat Dec 16 04:29:16 GMT 2023 , Edited by admin on Sat Dec 16 04:29:16 GMT 2023
|
PRIMARY | |||
|
12743
Created by
admin on Sat Dec 16 04:29:16 GMT 2023 , Edited by admin on Sat Dec 16 04:29:16 GMT 2023
|
PRIMARY | |||
|
211-756-8
Created by
admin on Sat Dec 16 04:29:16 GMT 2023 , Edited by admin on Sat Dec 16 04:29:16 GMT 2023
|
PRIMARY | |||
|
DTXSID4022105
Created by
admin on Sat Dec 16 04:29:16 GMT 2023 , Edited by admin on Sat Dec 16 04:29:16 GMT 2023
|
PRIMARY |