ISOPROPYLDIPHENYLPHOSPHINE

Product Information

Molecular Formula:
C15H17P
Molecular Weight:
228.27
Description
Catalyst in:• Nickel/Lewis acid-catalyzed aryl- and alkenylcyanation of unsaturated bonds• Nickel/Lewis Acid-Catalyzed Cyanoesterification and Cyanocarbamoylation of Alkynes• Methoxycarbonylation reactions (palladium complex)• Decarboxylative cross-coupling in the presence of palladium• Asymmetric hydrogenation of quinolines catalyzed by iridium complexes of BINOL-derived diphosphonites• Hydroesterification of vinylarenes in complex with palladium• Ligand precatalyst for room-temperature Heck coupling reactions
Synonyms
ISOPROPYLDIPHENYLPHOSPHINE; DIPHENYL-ISO-PROPYLPHOSPHINE; i-Propyldiphenylphosphine,99%; I-PROPYLDIPHENYLPHOSPHINE; Einecs 228-902-1; Phosphine, (1-methylethyl)diphenyl-
IUPAC Name
diphenyl(propan-2-yl)phosphane
Canonical SMILES
CC(C)P(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChI=1S/C15H17P/c1-13(2)16(14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-13H,1-2H3
InChI Key
LLZAIAIZAVMQIG-UHFFFAOYSA-N
Boiling Point
165 °C/11 mmHg (lit.)
Melting Point
40-43 °C (lit.)
Flash Point
235.4 °F - closed cup
Purity
>97.0%(GC)
Density
0.861

Safety Information

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

Computed Properties

XLogP3
3.9
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
3
Exact Mass
228.106787540 g/mol
Monoisotopic Mass
228.106787540 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
170
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
KR-20220022349-A (ALKYL)ARENES AND A Method for Producing the Same 2020-08-18
WO-2021230194-A1 Composition 2020-05-14
WO-2021230195-A1 Composition 2020-05-14
CN-111518145-A Cyanide-bridged metal organic compound with intramolecular magnetic transformation, and preparation method and application thereof 2020-05-07
WO-2021219418-A1 Preparation of aromatic carboxyamides by palladium-catalyzed carbonylation reaction 2020-04-29
WO-2021219424-A1 Preparation of aromatic carboxyamides by a palladium-catalyzed carbonylation reaction 2020-04-29
JP-2021161333-A Polycarbonate resin composition and its molded product 2020-04-02
DE-202020001249-U1 Hydroxyalkyl acrylate based monomers for use as reactive diluents in printing formulations 2020-04-01
JP-2021138910-A Modified epoxidized polybutadiene, epoxy resin composition and cured product and can paint and can coating 2020-03-06
KR-20210101082-A (arylmethyl)arenes and a production process thereof 2020-02-07

Literatures

PMID Publication Date Title Journal
5789 1976-04-01 Hyperoxia and red cell 2,3-diphosphoglycerate Toxicology and applied pharmacology
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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