Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C3H5FO |
| Molecular Weight | 76.0696 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FCC1CO1
InChI
InChIKey=OIFAHDAXIUURLN-UHFFFAOYSA-N
InChI=1S/C3H5FO/c4-1-3-2-5-3/h3H,1-2H2
| Molecular Formula | C3H5FO |
| Molecular Weight | 76.0696 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Enantioselective binding of structural epoxide isomers by a chiral vanadyl salen complex: a pulsed EPR, cw-ENDOR and DFT investigation. | 2009-08-21 |
|
| A cold-adapted epoxide hydrolase from a strict marine bacterium, Sphingophyxis alaskensis. | 2008-08 |
|
| Aqueous-phase aminolysis: approach for the analysis of epoxides in water. | 2006-04-15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:50:12 GMT 2025
by
admin
on
Mon Mar 31 21:50:12 GMT 2025
|
| Record UNII |
0ZZ4ROH5IL
|
| Record Status |
Validated (UNII)
|
| Record Version |
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-
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207-960-1
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DTXSID4025244
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88608
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21303
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503-09-3
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10418
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0ZZ4ROH5IL
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