Palladium(2+) acetate triphenylphosphine (1:2:2)

Basic Information

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CAS Number

14588-08-0

Molecular Formula

C40H36O4P2Pd

Molecular Weight

751.11 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Fine Chemicals Dyes and Pigments Organic Dyes

Fine Chemicals Surfactants Anionic Surfactants

Agricultural Chemicals Pesticides Insecticides

Basic Physical Properties

Melting Point

136 °C (dec.)

SMILES

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CC(=O)[O-].CC(=O)[O-].C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.[Pd+2]

InChI

InChI=1S/2C18H15P.2C2H4O2.Pd/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;2*1-2(3)4;/h2*1-15H;2*1H3,(H,3,4);/q;;;;+2/p-2

InChIKey

UVBXZOISXNZBLY-UHFFFAOYSA-L

LogP

6.379300000000008

Topological Polar Surface Area

52.6 Å²

Hydrogen Bond Donor/Acceptor

0 / 4

Complexity

227

Safety Information

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Hazard Statement

H315 Causes skin irritation
Skin corrosion/irritation

H319 Causes serious eye irritation
Serious eye damage/eye irritation

H335 May cause respiratory irritation
Specific target organ toxicity, single exposure; Respiratory tract irritation

Stability

store cold

Sensitiveness

对空气及热敏感

Synonyms & References

English

B2042
Palladium(2+) acetate--triphenylphosphane (1/2/2)
bis(triphenylphosphine)-palladium(ii) acetate
bis(acetato)bis(triphenylphosphine)-palladium(II)
bis(triphenylphosphine) palladium (II) acetate
AKOS015898550
DTXSID00932711
UVBXZOISXNZBLY-UHFFFAOYSA-L
bis(triphenylphosphine)-palladium-(ii) acetate
palladium(2+) ion bis(triphenylphosphane) diacetate
Bis(triphenylphosphinepalladium) acetate
BCP21891
di(triphenylphosphine) diacetoxypalladium
bis(triphenyl phosphine)palladium(ii) acetate
J-519895
bis(triphenylphosphine)-palladium (II) acetate
bis(triphenylphosphine)palladium(ii) acetate
bis(acetato) bis(triphenylphosphine)palladium (II)
14588-08-0
bis(triphenylphoshine)palladium(II)acetate
bis(triphenylphosphine) palladium(II)acetate
bis(triphenylphosphine) palladium(ii) acetate
DS-2316
Palladium(II)bis(triphenylphosphine) diacetate
AMY39368
bis(acetato)bis(triphenylphosphine)palladium (II)
EINECS 238-628-4
Bis(triphenylphosphine)palladium(II) diacetate
bis(triphenylphosphine) palladium diacetate
D77929
Bis(acetato)bis(triphenylphosphine)palladium(II)

MDL Number

MFCD00010013

FAQ

What are the physical and chemical properties of Palladium(2+) acetate triphenylphosphine (CAS: 14588-08-0)?

Palladium(2+) acetate triphenylphosphine (CAS: 14588-08-0) is a crystalline compound with a molecular weight of approximately 541.28. It is sparingly soluble in water but highly soluble in organic solvents such as ethanol and acetone. This compound exhibits high reactivity towards carbon-hydrogen bonds, making it an excellent catalyst in cross-coupling reactions. It is often used in palladium-catalyzed C-H activation reactions.

How is Palladium(2+) acetate triphenylphosphine (CAS: 14588-08-0) typically synthesized?

Palladium(2+) acetate triphenylphosphine is typically synthesized by reacting palladium acetate with triphenylphosphine in an inert solvent like toluene or ethyl acetate. The process involves careful control of temperature and stirring rate to achieve good yield and selectivity. Catalysts like Pd(PPh3)4 are commonly used to enhance the reaction efficiency.

What industries use Palladium(2+) acetate triphenylphosphine (CAS: 14588-08-0)?

Palladium(2+) acetate triphenylphosphine (CAS: 14588-08-0) is widely used in the pharmaceuticals industry for the synthesis of complex molecules and in the polymer industry for the preparation of functional polymers. It also finds applications in the electronics industry for semiconductor fabrication and in sensor technology for detecting various chemical species.

What precautions should be taken when handling Palladium(2+) acetate triphenylphosphine (CAS: 14588-08-0)?

When handling Palladium(2+) acetate triphenylphosphine (CAS: 14588-08-0), it is essential to wear appropriate personal protective equipment (PPE) including gloves, safety goggles, and a laboratory coat. Work should be conducted in a well-ventilated area or a fume hood to avoid inhalation. Spills should be cleaned up immediately using appropriate absorbent materials and proper disposal methods. Always refer to the safety data sheet (SDS) for detailed guidelines on handling and storage.