(+)-3-(Trifluoroacetyl)camphor, 98%

Code: 189006-1G D2-231

Application

(+)-3-(Trifluoroacetyl)camphor reacts with suitable chiral ketone precursors to generate chiral dioxiranes in situ, which can catalyse the direct asymmetric epoxi...


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Application

(+)-3-(Trifluoroacetyl)camphor reacts with suitable chiral ketone precursors to generate chiral dioxiranes in situ, which can catalyse the direct asymmetric epoxidation of unfunctionalized olefins.

Packaging

1 g in glass bottle

assay98%
bp100-101 °C/16 mmHg (lit.)
density1.172 g/mL at 25 °C (lit.)
formliquid
InChI keyISLOIHOAZDSEAJ-XGLFCGLISA-N
InChI1S/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
optical activity[α]19/D +148°, c = 2.3 in methylene chloride
refractive indexn20/D 1.451 (lit.)
SMILES stringCC1(C)C2CC[C@@]1(C)C(=O)C2C(=O)C(F)(F)F
Cas Number51800-98-7
This product has met the following criteria: