Allyldiphenylphosphine

Product Information

Molecular Formula:
C15H15P
Molecular Weight:
226.2534
Description
• Cocatalyst in palladium catalyzed hydrocarboxylation reactions• Cocatalyst in Palladium catalyzed cross-coupling reactions• Ligand for hydroformylation catalysts• Ligand for the rhenium phosphinoborane pendant Lewis acid-assisted reductive coupling reactions• Catalyst precursor for alkene hydroboration
Synonyms
DIPHENYL-2-PROPENYLPHOSPHINE; DIPHENYLALLYLPHOSPHINE; ALLYLDIPHENYLPHOSPHINE; ALLYLDIPHENYLPHOSPHINE, TECH., 80%; 2-Propenyldiphenylphosphine; Allyldiphenylphosphine,80%,tech.; Diphenylphosphino
IUPAC Name
diphenyl(prop-2-enyl)phosphane
Canonical SMILES
C=CCP(C1=CC=CC=C1)C2=CC=CC=C2
InChI
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
InChI Key
PDDYFPPQDKRJTK-UHFFFAOYSA-N
Boiling Point
194-200 °C/15 mmHg (lit.)
Flash Point
235.4 °F - closed cup
Purity
95%
Density
1.049
Refractive Index
n20/D 1.619 (lit.)

Safety Information

Hazards
H315 - H319 - H335
Precautionary Statement
P302 + P352 - P305 + P351 + P338

Computed Properties

XLogP3
3.7
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
4
Exact Mass
226.091137476 g/mol
Monoisotopic Mass
226.091137476 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
182
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113402416-A Preparation method of methoxylamine hydrochloride 2021-05-29
WO-2022003040-A1 Process for treating keratin fibers using particular amino acids in high concentration 2020-06-30
JP-2021185399-A Quantum dot-containing polymer and its manufacturing method 2020-05-25
WO-2021241071-A1 Quantum dot-containing polymer and method for producing same 2020-05-25
CN-111518145-A Cyanide-bridged metal organic compound with intramolecular magnetic transformation, and preparation method and application thereof 2020-05-07
CN-113402665-A Dental photocurable composition comprising highly soluble photoacid generator 2020-03-16
CN-113402666-A Dental photocurable composition with excellent color tone selectivity 2020-03-16
EP-3888615-A1 Dental photocurable composition containing high soluble photoacid generator 2020-03-16
EP-3888616-A1 Dental photocurable composition excellent in color tone selectivity 2020-03-16
WO-2021099522-A1 Methods for coupling a ligand to a composite material 2019-11-21

Literatures

PMID Publication Date Title Journal
20872381 2010-11-22 Imidazoliophosphines are true N-heterocyclic carbene (NHC)-phosphenium adducts Chemistry (Weinheim an der Bergstrasse, Germany)
16856202 2006-07-24 Substituted allyl diphenylphosphine oxides as radical allylating agents Angewandte Chemie (International ed. in English)
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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