Bis(tri-t-butylphosphine)palladium structure
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Common Name | Bis(tri-t-butylphosphine)palladium | ||
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CAS Number | 53199-31-8 | Molecular Weight | 511.05 | |
Density | N/A | Boiling Point | 229.4ºC at 760mmHg | |
Molecular Formula | C24H54P2Pd | Melting Point | >300 °C | |
MSDS | Chinese USA | Flash Point | 94.6ºC |
Use of Bis(tri-t-butylphosphine)palladiumBis(tri-tert-butylphosphine)palladium(0) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | Bis(tri-tert-butylphosphine)palladium(0) |
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Synonym | More Synonyms |
Description | Bis(tri-tert-butylphosphine)palladium(0) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Boiling Point | 229.4ºC at 760mmHg |
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Melting Point | >300 °C |
Molecular Formula | C24H54P2Pd |
Molecular Weight | 511.05 |
Flash Point | 94.6ºC |
Exact Mass | 510.273560 |
PSA | 27.18000 |
LogP | 9.72760 |
Storage condition | Freezer |
Water Solubility | insoluble |
Pd/P(t-Bu)(3): a mild and general catalyst for Stille reactions of aryl chlorides and aryl bromides.
J. Am. Chem. Soc. 124 , 6343, (2003) Pd/P(t-Bu)(3) serves as an unusually reactive catalyst for Stille reactions of aryl chlorides and bromides, providing solutions to a number of long-standing challenges. An unprecedented array of aryl ... |
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Sequential assembly strategy for tetrasubstituted olefin synthesis using vinyl 2-pyrimidyl sulfide as a platform.
J. Am. Chem. Soc. 126 , 11778, (2004) We have developed a programmable and diversity-oriented synthetic scheme for tetrasubstituted olefins through a site-selective and sequential assembly of pi-components onto a C=C core of vinyl 2-pyrim... |
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Aqueous hydroxide as a base for palladium-catalyzed amination of aryl chlorides and bromides.
J. Org. Chem. 67 , 6479, (2002) The amination of aryl halides in the presence of inexpensive and air-stable alkali metal hydroxide bases and Pd[P(t-Bu)3]2 as catalyst gave arylamines in high yields. The reactions were conducted with... |
palladium,tritert-butylphosphane |
palladium - tri-tert-butylphosphane (1:2) |
Bis(tri-t-butylphosphine)palladium |
Palladium - tri-tert-butylphosphine (1:2) |
Pd(t-Bu3P)2 |
MFCD03094580 |
Bis(tri-t-butylphosphine)palladium(0) |
Palladium - tris(2-methyl-2-propanyl)phosphine (1:2) |
Phosphine, tris(1,1-dimethylethyl)-, palladium salt (2:1) |