Application：3-(Trifluoroacetyl)-D-camphor reacts with suitable chiral ketone precursors to generate chiral epoxyethane in situ, which can catalyze the direct asymmetric epoxidation of unfunctionalized olefins.
- Properties
- Weights
- Citation
| Name | (+)-3-(Trifluoroacetyl)camphor |
|---|---|
| CasNumber | 51800-98-7 |
| GradePurity | ≥98% |
| Formula | C12H15F3O2 |
| MolecularWeight | 248.24 |
| IupacName | |
| Smiles | CC1(C2CCC1(C(=O)C2C(=O)C(F)(F)F)C)C |
| InchiKey | ISLOIHOAZDSEAJ-XGLFCGLISA-N |
| Inchi | 1S/C12H15F3O2/c1-10(2)6-4-5-11(10,3)8(16)7(6)9(17)12(13,14)15/h6-7H,4-5H2,1-3H3/t6-,7?,11+/m1/s1 |
| Synonyms | (+)-3-(Trifluoroacetyl)camphor | EINECS 257-429-3 | (+)-3-(Trifluoroacetyl)camphor, 98% | 1,7,7-Trim... |
| CidNumber |
| SKU | Size | Unit | Price $ | Stock | |
|---|---|---|---|---|---|
| T170745-250mg | 250 | mg | 72 | 3 | |
| T170745-1g | 1 | g | 200 | 2 |
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