Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C9H20O |
| Molecular Weight | 144.2545 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCC(O)CC
InChI
InChIKey=GYSCXPVAKHVAAY-UHFFFAOYSA-N
InChI=1S/C9H20O/c1-3-5-6-7-8-9(10)4-2/h9-10H,3-8H2,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Solvent effect on ion-pair extraction of 2-(2-pyridylazo)-1-naphthol-4-sulfonate anion with solvated hydroxonium ion using alcohols and 1-octanol/octane mixed solvents. | 2001 Feb |
|
| Purification and characterization of a feruloyl esterase from Fusarium oxysporum catalyzing esterification of phenolic acids in ternary water-organic solvent mixtures. | 2003 Apr 10 |
|
| Esterification of phenolic acids catalyzed by lipases immobilized in organogels. | 2010 Oct |
Patents
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| Code System | Code | Type | Description | ||
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210-850-6
Created by
admin on Sat Dec 16 09:37:24 GMT 2023 , Edited by admin on Sat Dec 16 09:37:24 GMT 2023
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624-51-1
Created by
admin on Sat Dec 16 09:37:24 GMT 2023 , Edited by admin on Sat Dec 16 09:37:24 GMT 2023
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047779Z489
Created by
admin on Sat Dec 16 09:37:24 GMT 2023 , Edited by admin on Sat Dec 16 09:37:24 GMT 2023
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12216
Created by
admin on Sat Dec 16 09:37:24 GMT 2023 , Edited by admin on Sat Dec 16 09:37:24 GMT 2023
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DTXSID50862317
Created by
admin on Sat Dec 16 09:37:24 GMT 2023 , Edited by admin on Sat Dec 16 09:37:24 GMT 2023
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SUBSTANCE RECORD
