추천 제품
양식
powder
Quality Level
작용기
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
애플리케이션
- [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
법적 정보
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
이미 열람한 고객
문서
Hydrogenation, Asymmetric Catalysis, Binap, SEGPHOS®, Aldol reaction, Alkenylation, Arylation, Mannich reaction, Fluorination, Michael addition, Hydrosilylation, Cycloaddition, Takasago
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