palladium(II) chloride, Promotion Season Now in Store and Free Sample for Testing with Factory Price
- Chemical Name: Bis(triphenylphosphine)palladium(II) chloride
- CAS No.: 13965-03-2
- Molecular Fomula: : C36H30Cl2P2Pd
- Molecular weight:701.9
- Appearance: yellow powder
- Sample:Available
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Description of palladium(II) chloride
Bis(triphenylphosphine)palladium chloride is a coordination compound of palladium containing two triphenylphosphine and two chloride ligands. It is a yellow solid that is soluble in some organic solvents. It is used for palladium-catalyzed coupling reactions, e.g. the Sonogashira–Hagihara reaction. The complex is square planar. Both cis and trans isomers are known. Many analogous complexes are known with different phosphine ligands.
Basic Info of palladium(II) chloride
Basic Info
Numbering system
Properties
Safety Info
Basic Info
Chemical Name |
Bis(triphenylphosphine)palladium(II) chloride |
Synonyms |
(Ph3P)2Pd(II)Cl2;Bis(triphenylphosphine)palladium Chloride;PdCl2(PPh3)2;trans-dichlorobis(triphenylphosphine)palladium (II);Dichlorobis(triphenylphosphine)palladium(II);Expand |
CAS No. |
13965-03-2 |
Molecular Formula |
C36H30Cl2P2Pd |
Molecular Weight |
701.89700 |
PSA |
27.18000 |
LogP |
8.26860 |
Numbering system
MDL number |
MFCD00009593 |
BRN number |
4935975 |
EINECS number |
237-744-2 |
PubChem number |
24849233 |
Properties
Appearance & Physical State |
yellow crystals. |
Boiling Point |
360ºC at 760 mmHg |
Melting Point |
260ºC |
Flash Point |
181.7ºC |
Stability |
Stable at room temperature in closed containers under normal storage and handling conditions. |
Storage Condition |
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. Store protected from moisture. |
Safety Info
Safety Statements |
S26-S37/39 |
HS Code |
28439090 |
WGK Germany |
3 |
Risk Statements |
R22; R36/37/38 |
Hazard Codes |
Xn |
Supplemental Hazard Statements |
May form explosive peroxides. |
Signal Word |
Warning |
Symbol |
GHS08 |
Caution Statement |
P281 |
Hazard Declaration |
H351 |
What is Bis(triphenylphosphine)palladium(II) chloride?
- With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is Bis(triphenylphosphine)palladium(II) chloride which has developed particularly rapidly in recent years. Do you know about Bis(triphenylphosphine)palladium(II) chloride ?
- The official answer:Bis(triphenylphosphine)palladium dichloride is a chemical substance with the molecular formula C36H30Cl2P2Pd. Bis(triphenylphosphine)palladium dichloride is insoluble in water. Soluble in toluene, benzene, slightly soluble in acetone, chloroform. The melting point is 260 degrees C. It is mainly used as a catalyst for coupling reactions such as Sonogoshira coupling, the catalyst for carbonylation of halogenated substances, halogenated alkanes to make aldehydes, carboxylic acids, amides, etc., and halogenated alkanes react with acetylene to form alkyne compounds with growing carbon chains.
What’s the application ofBis(triphenylphosphine)palladium(II) chloride?
- Bis(triphenylphosphine)palladium(II) dichloride is a chemical substance. Bis(triphenylphosphine)palladium(II) chloride is used as a catalyst for organic synthesis, mostly in Suzuki reactions. Carboxylic acids can be decarboxylated to form α-alkenes catalyzed by catalytic amounts of bis(triphenylphosphine)palladium(II) chloride, which is used as a catalyst in Suzuki, Kumada, Negishi, and other coupling reactions. Due to a certain amount of palladium, dichloro bis(triphenylphosphine)palladium(II) is mainly used in organometallic catalytic reactions. It is also involved in the crystalline structure of metal ring complexes, showing anti-inflammatory and antifungal properties, and is mainly used in coupling reactions such as Sonogoshira coupling; carbonylation catalyst of halogenated substances; halogenated alkanes to make aldehydes, carboxylic acids, amides, etc.; halogenated alkanes react with acetylene to form alkyne compounds with growing carbon chains.
Conclusion
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