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线性分子式:
[(C6H5)2PC10H6-]2
化学文摘社编号:
分子量:
622.67
UNSPSC Code:
12352005
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5321443
InChI
1S/C44H32P2/c1-5-19-35(20-6-1)45(36-21-7-2-8-22-36)41-31-29-33-17-13-15-27-39(33)43(41)44-40-28-16-14-18-34(40)30-32-42(44)46(37-23-9-3-10-24-37)38-25-11-4-12-26-38/h1-32H
InChI key
MUALRAIOVNYAIW-UHFFFAOYSA-N
grade
puriss.
form
solid
optical activity
[α]20/D −239±5°, c = 0.3% in toluene
optical purity
enantiomeric ratio: ≥99.5:0.5 (HPLC)
mp
238-240 °C (lit.), 238-242 °C (dec.)
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Application
作为以下过程的反应物:
- 对映选择性和非对映选择性非极化羰基烯丙基化
- 合成有机膦氧化物,作为抗肿瘤药
- 羟基的SN2卤化
- 合成BINAP配合物
- BINAP螯合物的构象灵活性研究
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
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)
法规信息
新产品
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Kim-Hung Lam et al.
European journal of medicinal chemistry, 45(11), 5527-5530 (2010-09-14)
Following our previously reported pyridinyl phosphine oxides as antitumor agents, we targeted the commercially available C(2)-axial chiral organophosphine ligand catalysts, such as 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (BINAP) 1 and 2,2',6,6'-tetramethoxy-4,4'-bis(diphenylphosphino)-3,3'-bipyridine (P-Phos) 2 as a convenient source for producing organophosphine oxides as antitumor leads.
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