693456
史氏环氧化恶唑烷酮甲基催化剂
95%
别名:
(3aR,5′S,7aR)-二氢-2,2-二甲基-3′-(4-甲基苯基)-螺[6H-1,3-二氧并[4,5-c]吡喃-6,5′-噁唑烷]-2′,7(4H)-二酮
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关于此项目
经验公式（希尔记法）:
C17H19NO6
化学文摘社编号:
分子量:
333.34
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
产品名称
史氏环氧化恶唑烷酮甲基催化剂, 95%
InChI
1S/C17H19NO6/c1-10-4-6-11(7-5-10)18-9-17(24-15(18)20)14(19)13-12(8-21-17)22-16(2,3)23-13/h4-7,12-13H,8-9H2,1-3H3/t12-,13-,17+/m1/s1
SMILES string
Cc1ccc(cc1)N2C[C@]3(OC[C@H]4OC(C)(C)O[C@H]4C3=O)OC2=O
InChI key
WFKGDVVGAWYPFR-XNJGSVPQSA-N
assay
95%
form
solid
optical activity
[α]22/D -28.0°, c = 1 in chloroform
mp
149-154 °C
functional group
ether
ketal
ketone
storage temp.
2-8°C
Quality Level
Application
不对称环氧化有机催化剂
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
商品
Catalytic asymmetric epoxidation of alkenes has been the focus of many research efforts over the past two decades, the best known methods probably being those developed by Sharpless and Jacobsen-Katsuki.
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