Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C19H38O3 |
| Molecular Weight | 314.5032 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCC(O)CCCCCCCCCCC(=O)OC
InChI
InChIKey=RVWOWEQKPMPWMQ-UHFFFAOYSA-N
InChI=1S/C19H38O3/c1-3-4-5-12-15-18(20)16-13-10-8-6-7-9-11-14-17-19(21)22-2/h18,20H,3-17H2,1-2H3
| Molecular Formula | C19H38O3 |
| Molecular Weight | 314.5032 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Lipase-catalyzed synthesis and properties of poly[(12-hydroxydodecanoate)-co-(12-hydroxystearate)] directed towards novel green and sustainable elastomers. | 2008-01-09 |
|
| 1-phenylethyl isocyanate is a powerful reagent for the chiral analysis of secondary alcohols and hydroxy fatty acids with remote stereogenic centres. | 2007-09-21 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:02:12 GMT 2025
by
admin
on
Mon Mar 31 21:02:12 GMT 2025
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| Record UNII |
P7UC7KGL82
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Validated (UNII)
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