Diphenyl(p-tolyl)phosphine

Product Information

Molecular Formula:
C19H17P
Molecular Weight:
276.312
Description
Reactant for:• Three-component cyclization• Probing coordination ability via a palladium pincer complex• Chelation-assisted hydroacylation of olefins with primary alcoholsReactant for synthesis of:• Trinuclear ruthenium carbonyl triarylphosphine cluster complexes• Leishmanicidal leads targeting mitochondria through inhibition of the respiratory complex• InP nanofibers / metal phosphide nanostructures• Peroxyl radical cations via pulse radiolysis one-electron oxidations
Synonyms
P-TOLYLDIPHENYLPHOSPHINE; Phosphine, (4-methylphenyl)diphenyl-; DIPHENYL(P-TOLYL)PHOSPHINE; DIPHENYL-4-TOLYLPHOSPHINE; DIPHENYL-4-METHYLPHENYLPHOSPHINE; (4-METHYLPHENYL)(DIPHENYL)PHOSPHINE; p-Tolyldiphenylphosphine,min.96%; p-Tolyldiphenylphosphine, 96+%
IUPAC Name
(4-methylphenyl)-diphenylphosphane
Canonical SMILES
CC1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChI=1S/C19H17P/c1-16-12-14-19(15-13-16)20(17-8-4-2-5-9-17)18-10-6-3-7-11-18/h2-15H,1H3
InChI Key
QJIMTLTYXBDJFC-UHFFFAOYSA-N
Melting Point
66-68 °C (lit.)
Flash Point
Not applicable
Purity
96%
Appearance
white to light yellow crystal powde

Safety Information

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

Computed Properties

XLogP3
5
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
3
Exact Mass
276.106787540 g/mol
Monoisotopic Mass
276.106787540 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
20
Formal Charge
0
Complexity
250
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-113149882-A Gem-difluoroolefin-pyrroline compound and preparation method and application thereof 2021-02-05
JP-6870778-B1 Resin composition for molding and electronic component equipment 2020-12-11
JP-2022021901-A A resin composition for encapsulation, an electronic component device, and a method for manufacturing the electronic component device. 2020-07-22
JP-2022021902-A A resin composition for encapsulation, an electronic component device, and a method for manufacturing the electronic component device. 2020-07-22
WO-2022009930-A1 Light-emitting material, light-emitting ink, light-emitting body, and light-emitting device 2020-07-10
WO-2022003040-A1 Process for treating keratin fibers using particular amino acids in high concentration 2020-06-30
JP-2022011184-A Encapsulating resin composition and electronic component equipment 2020-06-29
JP-2022007673-A Manufacturing method of sealing resin composition, sealing resin composition, manufacturing method of electronic component equipment, and electronic component equipment 2020-06-26
CN-111689847-A Preparation method of aryl propionic acid compound 2020-06-12
US-2021371441-A1 Platinum complex, its preparation and therapeutic use 2020-05-22

Literatures

PMID Publication Date Title Journal
21724304 2011-09-01 Synthesis, characterization and anticancer studies of mixed ligand dithiocarbamate palladium(II) complexes European journal of medicinal chemistry
20023954 2010-01-07 Synthesis of InP nanofibers from tri(m-tolyl)phosphine: an alternative route to metal phosphide nanostructures Dalton transactions (Cambridge, England : 2003)
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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