Substance
ID:339420
Names and Identifiers
IUPAC Traditional name
chloroform tris(dibenzylideneacetone) dipalladium
Synonyms
三(二亚苄基丙酮)二钯(0)-氯仿加合物Pd2(dba)3 · CHCl3Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct三(二亚苄基丙酮)二钯-氯仿络合物Dipalladium-tris(dibenzylideneacetone)chloroform complex
IUPAC name
tris(1,5-diphenylpenta-1,4-dien-3-one) trichloromethane dipalladium
Properties
Safety Information
GHS Hazard statements
H302-H315-H351
German water hazard class
3
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
European Hazard Symbols
Harmful (Xn)MSDS Link
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Signal Word
Warning
Risk Statements
22-38-40
Safety Statements
36/37
GHS Precautionary statements
P281
Product Information
Linear Formula
(C6H5CH=CHCOCH=CHC6H5)3Pd2 · CHCl3
Physical Property
Melting Point
131-135 °C(lit.)
Molecule Details
Packaging
1 g in glass bottle
250 mg in glass bottle
Application
Application Guide for Palladium Catalyzed Cross-Coupling Reactions
Cyclization catalyst.Catalyst for [2+2+2] cycloaddtion of didehydrotriphenylenes to the corresponding extended triphenylenes. Catalyst for the carbonylation of b,b-imidoyl iodides to the corresponding imidate esters used, in turn, to prepare cyclic, quaternary amino acids.
1 g in glass bottle
250 mg in glass bottle
Application
Application Guide for Palladium Catalyzed Cross-Coupling Reactions
Cyclization catalyst.Catalyst for [2+2+2] cycloaddtion of didehydrotriphenylenes to the corresponding extended triphenylenes. Catalyst for the carbonylation of b,b-imidoyl iodides to the corresponding imidate esters used, in turn, to prepare cyclic, quaternary amino acids.
Molecular Spectra
No Data Available
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References
No Data Available
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