97858-62-3(S,S)-双[(2-甲氧基苯基)苯基磷]乙烷,97%
- 发布日期: 2018-09-21
- 更新日期: 2026-02-09
产品详请
| 产地 |
中国/美国/欧洲
|
| 品牌 |
LMAI Bio
|
| 货号 |
LM002465
|
| 包装规格 |
100mg 250mg
|
| 纯度 |
99%
|
| CAS编号 |
97858-62-3
|
| 别名 |
(S,S)-1,2-双[(2-甲氧基苯基)苯基膦基]乙烷;
|
97858-62-3(S,S)-双[(2-甲氧基苯基)苯基磷]乙烷,97%
CAS号: 97858-62-3
分子式: C28H28O2P2 分子量: 458.47

(S,S)-双[(2-甲氧基苯基)苯基磷]乙烷
英文名:(S,S)-DIPAMP
| CAS: | 97858-62-3 | 精确质量: | 458.15600 |
| 分子式: | C28H28O2P2 | LogP: | 5.26940 |
| 分子量: | 458.46800 | PSA: | 45.64000 |
97858-62-3(S,S)-双[(2-甲氧基苯基)苯基磷]乙烷,97%化合物描述
DIPAMP is an organophosphorus compound that is used as a ligand in homogeneous catalysis. It is a white solid that dissolves in organic solvents. Work on this compound by W. S. Knowles was recognized with the Nobel Prize in Chemistry. DIPAMP was the basis for of the first industrial scale asymmetric hydrogenation, the synthesis of the drug L-DOPA.
DIPAMP is a chelating diphosphine. Each phosphorus centre, which is pyramidal, bears three different substituents - anisyl, phenyl, and the ethylene group. It therefore exists as the enantiomeric (R,R) and (S,S) pair, as well as the achiral meso isomer.
DIPAMP was originally prepared by an oxidative coupling reaction, starting from anisyl(phenyl)(methyl)phosphine.
97858-62-3(S,S)-双[(2-甲氧基苯基)苯基磷]乙烷,97%基本信息
中文名称:
(S,S)-双[(2-甲氧基苯基)苯基磷]乙烷
中文别名:
(S,S)-1,2-双[(2-甲氧基苯基)苯基膦基]乙烷;
英文名称:
(S,S)-DIPAMP
英文别名:
1,2-bis[(o-methoxyphenyl)phenylphosphino]ethane;
(R,R)-1,2-Bis[(o-methoxyphenyl)phenylphosphino]ethane;
2-(2,3-Epoxy-propoxy)-m-xylol;
(+/-)-1,2-ethandiylbis[(o-anisylphenyl)phenyl]phosphine;
2-((2,6-dimethylphenoxy)methyl)oxirane;
2-(2,3-epoxy-propoxy)-m-xylene;
(+/-)-1,2-epoxy-3-(2,6-dimethylphenoxy)propane;
2,6-dimethylphenyl glycidyl ether;
1,2-bis[(2-methoxyphenyl)(phenyl)phosphino]ethane;
(2,6-dimethyl-phenoxymethyl)-oxirane;
1,2-ethanediylbis[(o-anisylphenyl)phenylphosphine];
CAS号:
97858-62-3
分子式:
C28H28O2P2
分子量:
458.46800
精确质量:
458.15600
PSA:
45.64000
LogP:
5.26940
物化性质
熔点:
102-103oC
沸点:
580.2oC at 760mmHg