155039
Diphenyl(p-tolyl)phosphine
96%
Synonym(s):
(4-Methylphenyl)diphenyl phosphine
About This Item
Recommended Products
Assay
96%
form
liquid
reaction suitability
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
mp
66-68 °C (lit.)
functional group
phosphine
SMILES string
Cc1ccc(cc1)P(c2ccccc2)c3ccccc3
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
Application
- Three-component cyclization
- Probing coordination ability via a palladium pincer complex
- Chelation-assisted hydroacylation of olefins with primary alcohols
Reactant 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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service