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经验公式(希尔记法):
C32H22F10N2O2
化学文摘社编号:
分子量:
656.51
MDL number:
UNSPSC Code:
12161600
NACRES:
NA.22
产品名称
Berkessel ligand, 98%
SMILES string
Fc1c(c(c(c(c1F)F)c2c(c(ccc2)CN[C@@H]3[C@@H](CCCC3)\N=C\c4c(c(ccc4)c5c(c(c(c(c5F)F)F)F)F)O)O)F)F
InChI
1S/C32H22F10N2O2/c33-21-19(22(34)26(38)29(41)25(21)37)15-7-3-5-13(31(15)45)11-43-17-9-1-2-10-18(17)44-12-14-6-4-8-16(32(14)46)20-23(35)27(39)30(42)28(40)24(20)36/h3-8,11,17-18,44-46H,1-2,9-10,12H2/b43-11+/t17-,18+/m1/s1
InChI key
NLJCGFOPEQFWQJ-XOZUKITKSA-N
assay
98%
form
powder or crystals
reaction suitability
reagent type: ligand
Quality Level
Application
Developed by Albrecht Berkessel′s lab, this is the first catalyst system that allows catalytic enantioselective epoxidation of non-conjugated terminal double bonds with hydrogen peroxide as the oxidant. Eradicating multiple steps and kinetic resolution, this chiral ligand, when used with Ti(OiPr)4 provides a one-step route to enantiopure epoxides that are important intermediates for synthesis of bioactive compounds. Catalyst is recyclable under some conditions. For best results, pentafluorobenzoic acid (P5360) or tetra-n-butylammonium hydrogensulfate (155837) is recommended as a co-catalyst.
存储类别
11 - Combustible Solids
wgk
WGK 3
法规信息
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