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
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) |
