Details
Stereochemistry | RACEMIC |
Molecular Formula | C12H22O2 |
Molecular Weight | 198.3019 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCC(CC)COC(=O)C(C)=C
InChI
InChIKey=WDQMWEYDKDCEHT-UHFFFAOYSA-N
InChI=1S/C12H22O2/c1-5-7-8-11(6-2)9-14-12(13)10(3)4/h11H,3,5-9H2,1-2,4H3
Molecular Formula | C12H22O2 |
Molecular Weight | 198.3019 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Use of salt hydrate pairs to control water activity for enzyme catalysis in ionic liquids. | 2003 May-Jun |
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Ultrasound initiated miniemulsion polymerization of methacrylate monomers. | 2008 Jan |
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Development of new bone cement utilizing low toxicity monomers. | 2008 Jun |
|
Hydrolysis of p-nitrophenyl esters promoted by semifluorinated quaternary ammonium polymer latexes and films. | 2010 Oct 19 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 20:19:18 GMT 2023
by
admin
on
Sat Dec 16 20:19:18 GMT 2023
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Record UNII |
8Q7XLQ325N
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Record Status |
Validated (UNII)
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Record Version |
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Food Contact Sustance Notif, (FCN No.) |
FCN NO. 1145
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