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51364-51-3,MFCD00013310
Catalog No.:AA0035PA

51364-51-3 | Tris(dibenzylideneacetone)dipalladium(0)

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$12.00   $8.00
- +
1g
98%
in stock  
$26.00   $18.00
- +
5g
98%
in stock  
$108.00   $75.00
- +
10g
98%
in stock  
$200.00   $140.00
- +
25g
98%
in stock  
$486.00   $340.00
- +
  • Technical Information
  • Properties
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0035PA
Chemical Name:
Tris(dibenzylideneacetone)dipalladium(0)
CAS Number:
51364-51-3
Molecular Formula:
C51H42O3Pd2
Molecular Weight:
915.7174
MDL Number:
MFCD00013310
SMILES:
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Properties
Properties
 
BP:
400.7°C at 760 mmHg  
Form:
Solid  
MP:
152-155°C  
Solubility:
Soluble in chlorinated solvents, benzene and THF.  
Stability:
Air & Moisture Sensitive  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
272  
Covalently-Bonded Unit Count:
5  
Defined Bond Stereocenter Count:
6  
Heavy Atom Count:
56  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
12  

Literature
Application
Tris(dibenzylideneacetone)dipalladium(0) (51364-51-3) is widely employed as a catalyst in various chemical synthesis reactions. Its application spans diverse transformations, including cross-coupling reactions, carbonylation reactions, and cycloaddition reactions. Specifically, it serves as a catalyst in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of biaryl compounds from aryl halides and boronic acids. Additionally, it is utilized in Heck reactions, enabling the coupling of aryl halides with alkenes to form substituted alkenes. Furthermore, Tris(dibenzylideneacetone)dipalladium(0) plays a pivotal role in Sonogashira coupling reactions, promoting the coupling of terminal alkynes with aryl or vinyl halides to yield alkynylated products. Its versatility, stability, and efficiency make it a valuable tool in organic synthesis, contributing to the rapid and selective formation of complex organic molecules for various applications in pharmaceuticals, materials science, and agrochemicals.
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SDS
Tags:51364-51-3 Molecular Formula|51364-51-3 MDL|51364-51-3 SMILES|51364-51-3 Tris(dibenzylideneacetone)dipalladium(0)