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关于此项目
线性分子式:
[(C6H5)2PC10H6-]2
化学文摘社编号:
分子量:
622.67
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
form
crystals
Quality Level
optical activity
[α]20/D +222°, c = 0.5% in benzene
mp
239-241 °C (lit.)
functional group
phosphine
SMILES string
c1ccc(cc1)P(c2ccccc2)c3ccc4ccccc4c3-c5c(ccc6ccccc56)P(c7ccccc7)c8ccccc8
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
Application
(R)-BINAP 与烯丙基氯化钯 (II) 二聚体反应生成 BINAP-钯催化剂,可催化 1,3-二酮的不对称烯丙基化反应生成手性 2,2-二烷基-1,3-二酮。也可用于制备手性稳定的铑纳米粒子,可作为催化剂用于苯乙烯和醋酸乙烯酯的不对称氢甲酰化反应。
Legal Information
与 Takasago 联合销售,仅供研究使用。
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
商品
Hydrogenation, Asymmetric Catalysis, Binap, SEGPHOS®, Aldol reaction, Alkenylation, Arylation, Mannich reaction, Fluorination, Michael addition, Hydrosilylation, Cycloaddition, Takasago
We present an article concerning BINAP/SEGPHOS® Ligands and Complexes.
RuHCl (diphosphine)(diamine): Catalyst Precursors for the Stereoselective Hydrogenation of Ketones and Imines1
Abdur-Rashid, Kamaluddin, Alan J. Lough, and Robert H. Morris
Organometallics, 20.6, 1047-1049 (2001)
Asymmetric Hydrogenation of 3?Oxo Carboxylates Using Binap?Ruthenium Complexes:(R)?(?)?Methyl 3?Hydroxybutanoate
Kitamura, Masato, et al.
Organic Syntheses, 1-1 (1993)
Centenary lecture. Chemical multiplication of chirality: science and applications
Noyori, Ryoji
Chemical Society Reviews, 18, 187-208 (1989)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 693065-100MG | 04061833550656 |
| 693065-500MG | 04061832768847 |