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Allyldiphenylphosphine

Catalog Number
ACM2741380-2
Product Name
Allyldiphenylphosphine
Structure
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CAS
2741-38-0
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Synonyms
Diphenyl-2-propenylphosphine
IUPAC Name
diphenyl(prop-2-enyl)phosphane
Molecular Weight
226.25
Molecular Formula
C15H15P
Canonical SMILES
C=CCP(C1=CC=CC=C1)C2=CC=CC=C2;
InChI
PDDYFPPQDKRJTK-UHFFFAOYSA-N
InChI Key
InChI=1S/C15H15P/c1-2-13-16(14-9-5-3-6-10-14)15-11-7-4-8-12-15/h2-12H,1,13H2
Boiling Point
194-200 °C at 15 mmHg(lit.)
Flash Point
>230 °F
Purity
98%+
Density
1.049 g/mL at 25 °C (lit.)
Appearance
Liquid
Complexity
182
Covalently-Bonded Unit Count
1
Exact Mass
226.091g/mol
Heavy Atom Count
16
Isomeric SMILES
C=CCP(C1=CC=CC=C1)C2=CC=CC=C2
Monoisotopic Mass
226.091g/mol
NSC Number
616248
Rotatable Bond Count
4
Topological Polar Surface Area
0A^2
Application
Allyldiphenylphosphine serves a multitude of roles in various chemical reactions and processes. As a colorless to light yellow liquid, it is predominantly utilized as a cocatalyst in palladium-catalyzed hydrocarboxylation and cross-coupling reactions, enhancing the efficiency and outcomes of these processes. In addition, it acts as a ligand for hydroformylation catalysts, facilitating the formation of aldehydes from alkenes and syngas. Furthermore, Allyldiphenylphosphine functions as a ligand in rhenium phosphinoborane pendant Lewis acid-assisted reductive coupling reactions, contributing to the synthesis of complex molecules. Lastly, it serves as a catalyst precursor in the hydroboration of alkenes, aiding in the addition of boron to carbon-carbon double bonds.
February 28, 2025

Exceptional Versatility for Catalysis Applications

Allyldiphenylphosphine from Alfa Chemistry is indispensable in our lab. It effectively enhances palladium-catalyzed reactions and serves as a key ligand in hydroformylation, markedly improving our research results. Highly recommend for any catalysis-based project!

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