Tris(dibenzylideneacetone)dipalladium(0) structure
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Common Name | Tris(dibenzylideneacetone)dipalladium(0) | ||
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CAS Number | 51364-51-3 | Molecular Weight | 915.72 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C51H42O3Pd2 | Melting Point | 152-155°C | |
MSDS | USA | Flash Point | N/A | |
Symbol |
GHS08 |
Signal Word | Warning |
Use of Tris(dibenzylideneacetone)dipalladium(0)Tris(dibenzylideneacetonyl)bis-palladium is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | Tris(dibenzylideneacetone)dipalladium |
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Synonym | More Synonyms |
Description | Tris(dibenzylideneacetonyl)bis-palladium 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 | |
In Vitro | N-myristoyltransferase-1 (NMT-2)抑制剂,用作Suzuki、Kumada、Negishi、Buchwald等偶联反应的催化剂。 |
Melting Point | 152-155°C |
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Molecular Formula | C51H42O3Pd2 |
Molecular Weight | 915.72 |
Exact Mass | 914.120361 |
PSA | 51.21000 |
LogP | 11.94690 |
Storage condition | 2-8°C |
Water Solubility | insoluble |
Efficient syntheses of [¹¹C]zidovudine and its analogs by convenient one-pot palladium(0)-copper(I) co-mediated rapid C-[¹¹C]methylation.
J. Labelled Comp. Radiopharm. 57(8) , 540-9, (2014) The nucleosides zidovudine (AZT), stavudine (d4T), and telbivudine (LdT) are approved for use in the treatment of human immunodeficiency virus (HIV) and hepatitis B virus (HBV) infections. To promote ... |
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Carborane-derived local anesthetics are isomer dependent.
ChemMedChem 10(1) , 62-7, (2014) Clinically there is a need for local anesthetics with a greater specificity of action on target cells and longer duration. We have synthesized a series of local anesthetic derivatives we call boronica... |
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Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides.
J. Am. Chem. Soc. 132 , 14076, (2010) The palladium-catalyzed conversion of aryl and vinyl triflates to aryl and vinyl halides (bromides and chlorides) has been developed using dialkylbiaryl phosphine ligands. A variety of aryl, heteroary... |
Spermine NONOate |
Tris(dibenzylideneacetone)dipalladium(0) |
EINECS 479-280-5 |
Pd2(dibenzylideneacetone)3*CHCl3 |
Pd2(dba)3 Pd2dba3 |
Tris(Dibenzylidenacetone)palladiuM (O) |
(1E,4E)-1,5-Diphenyl-1,4-pentadien-3-one - palladium (3:2) |
MFCD00013310 |
(1E,4E)-1,5-Diphenylpenta-1,4-dien-3-one - palladium (3:2) |
Tris(dlbenzylideneacetone)dipalladiuM(O) |
Tris(dibenzylideneac |
TRIS(BIBENZYLIDENEACETONE) DIPALLADIUM |
palladium(II) tris(dibenzylideneacetone) |
Tris(Dibenzylideneacetone)Dipalladium |
1,4-Pentadien-3-one, 1,5-diphenyl-, (1E,4E)-, palladium salt (3:2) |
Bis[tris(dibenzylideneacetone)palladium(0)] |
tris(dibenzylidineacetone)dipalladium(0) |
Tris(dibezylideneacetone)dipalladium |
Tris(dibenzylidenaceTone) dipalladium (O) |
tris(dibenzylidene-acetone)dipalladium(0) |
Pd2dba3 Pd2(dba)3 |
1,4-pentadien-3-one, 1,5-diphenyl-, compd. with (1E,4E)-1,5-diphenyl-1,4-pentadien-3-one, palladium salt (1:2:2) |
Pd2(dibenzylidenacetone)3 |
Tris(dibenzylidenaceton)dipalladium |
Pd2(dibenzylideneacetone)3 |