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关于此项目
经验公式(希尔记法):
C46H48O2P2
化学文摘社编号:
分子量:
694.82
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352112
MDL number:
Quality Level
assay
≥97% (31P-NMR)
optical purity
ee: ≥99%
functional group
phosphine
SMILES string
COc1cccc(P(c2cc(C)cc(C)c2)c3cc(C)cc(C)c3)c1-c4c(OC)cccc4P(c5cc(C)cc(C)c5)c6cc(C)cc(C)c6
InChI
1S/C46H48O2P2/c1-29-17-30(2)22-37(21-29)49(38-23-31(3)18-32(4)24-38)43-15-11-13-41(47-9)45(43)46-42(48-10)14-12-16-44(46)50(39-25-33(5)19-34(6)26-39)40-27-35(7)20-36(8)28-40/h11-28H,1-10H3
InChI key
IMUHNRWTDUVXOU-UHFFFAOYSA-N
Application
(R)-(6,6′-Dimethoxybiphenyl-2,2′-diyl)bis[bis(3,5-dimethylphenyl)phosphine] can be used as a ligand:
- In the synthesis of (S)-3-amino-4-methoxy-butan-1-ol, a key starting material for many pharmaceutical drugs.
- In the synthesis of 3-substituted indanones through the reductive Heck reaction of chalcones with various amines.
- In the palladium-catalyzed Tsuji-Trost cyclizations of aldehydes to yield vinylcyclopentane derivatives.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
与 Solvias AG 联合销售
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
Solvias MeOBIPHEP Ligands: State-of-the-art atropisomeric MeOBIPHEP ligands, also referred to as MeO-BIPHEP, originally developed by Roche, have an extraordinarily broad performance profile for many synthetic applications due to their modular ligand design.
Recent Advances in the Synthesis of Indanes and Indenes.
Gabriele B, et al.
Chemistry?A European Journal (2016)
Aldrich Chemfiles, 5(4), 4-4 null
Synthesis of chiral 3-substituted indanones via an enantioselective reductive-Heck reaction
Minatti A, et al.
The Journal of Organic Chemistry, 72(24), 9253-9258 (2007)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 29516-5G | 04061832622736 |
| 29516-1G | 04061826094761 |
| 29516-500MG | 04061832622729 |
| 29516-100MG | 04061832622712 |