692484
(R)-DTBM-SEGPHOS®
Synonym(s):
(R)-(−)-5,5′-Bis[di(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-4,4′-bi-1,3-benzodioxole, [(4R)-(4,4′-bi-1,3-benzodioxole)-5,5′-diyl]bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine]
About This Item
Recommended Products
form
powder
Quality Level
functional group
phosphine
SMILES string
P(c8cc(c(c(c8)C(C)(C)C)OC)C(C)(C)C)(c7cc(c(c(c7)C(C)(C)C)OC)C(C)(C)C)c1c(c6c(cc1)OCO6)c2c3c(ccc2P(c5cc(c(c(c5)C(C)(C)C)OC)C(C)(C)C)c4cc(c(c(c4)C(C)(C)C)OC)C(C)(C)C)OCO3
InChI
1S/C74H100O8P2/c1-67(2,3)47-33-43(34-48(61(47)75-25)68(4,5)6)83(44-35-49(69(7,8)9)62(76-26)50(36-44)70(10,11)12)57-31-29-55-65(81-41-79-55)59(57)60-58(32-30-56-66(60)82-42-80-56)84(45-37-51(71(13,14)15)63(77-27)52(38-45)72(16,17)18)46-39-53(73(19,20)21)64(78-28)54(40-46)74(22,23)24/h29-40H,41-42H2,1-28H3
InChI key
ZNORAFJUESSLTM-UHFFFAOYSA-N
Related Categories
Application
- [3,3]-Sigmatropic rearrangements using cyclopropane probes
- Asymmetric intramolecular hydroacylation of ketoaldehydes
Reactant involved in:
- The synthesis of gold-diphosphine complexes for use as catalysts
- Cycloaddition of allenenes to yield alkylidenecyclobutanes
Legal Information
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Articles
Hydrogenation, Asymmetric Catalysis, Binap, SEGPHOS®, Aldol reaction, Alkenylation, Arylation, Mannich reaction, Fluorination, Michael addition, Hydrosilylation, Cycloaddition, Takasago
Global Trade Item Number
SKU | GTIN |
---|---|
692484-50MG | 4061832624891 |
692484-100MG | 4061832624884 |
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