Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H12O3 |
| Molecular Weight | 132.1577 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCCCCC(O)=O
InChI
InChIKey=IWHLYPDWHHPVAA-UHFFFAOYSA-N
InChI=1S/C6H12O3/c7-5-3-1-2-4-6(8)9/h7H,1-5H2,(H,8,9)
| Molecular Formula | C6H12O3 |
| Molecular Weight | 132.1577 |
| 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 |
|---|---|---|
| Effect of composition of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) on growth of fibroblast and osteoblast. | 2005 Mar |
|
| Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry with size-exclusion chromatographic fractionation for structural characterization of synthetic aliphatic copolyesters. | 2006 |
|
| Degradation and controlled release behavior of epsilon-caprolactone copolymers in biodegradable antifouling coatings. | 2006 Mar |
|
| Enatiomerically pure hydroxycarboxylic acids: current approaches and future perspectives. | 2010 Jun |
|
| Histone deacetylase inhibitor vorinostat suppresses the growth of uterine sarcomas in vitro and in vivo. | 2010 Mar 4 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:41:45 GMT 2023
by
admin
on
Fri Dec 15 16:41:45 GMT 2023
|
| Record UNII |
3Y3OX37NM8
|
| Record Status |
Validated (UNII)
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| Record Version |
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1191-25-9
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DTXSID00152316
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3Y3OX37NM8
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14490
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17869
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