1031-93-2 | Diphenyl(p-tolyl)phosphine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$13.00	$9.00
5g	95%	in stock	$26.00	$18.00
10g	95%	in stock	$42.00	$29.00
25g	95%	in stock	$76.00	$53.00
100g	95%	in stock	$225.00	$157.00

Description

• Catalog Number: AB73076
• Chemical Name: Diphenyl(p-tolyl)phosphine
• CAS Number: 1031-93-2
• Molecular Formula: C19H17P
• Molecular Weight: 276.312
• MDL Number: MFCD00008543
• SMILES: Cc1ccc(cc1)P(c1ccccc1)c1ccccc1

Computed Properties

• Complexity: 250
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 20
• Rotatable Bond Count: 3
• XLogP3: 5

Upstream Synthesis Route

Diphenyl(p-tolyl)phosphine is a versatile organophosphorus compound widely used in chemical synthesis as a powerful ligand in transition metal catalysis. Its unique structure and properties make it a valuable tool in various organic transformations.When used as a ligand, Diphenyl(p-tolyl)phosphine forms coordination complexes with transition metals, enhancing their reactivity and selectivity in a range of catalytic reactions. These include cross-coupling reactions, hydrogenation reactions, and asymmetric catalysis. The presence of the phosphine group facilitates the coordination of the metal center with the substrate, enabling efficient bond formation and cleavage processes.In addition to its role as a ligand, Diphenyl(p-tolyl)phosphine can also act as a reducing agent in certain reactions, enabling the conversion of functional groups under mild conditions. Its ability to participate in electron transfer processes expands its utility in various synthetic pathways, offering chemists greater flexibility in designing efficient synthetic routes.Overall, Diphenyl(p-tolyl)phosphine plays a crucial role in modern organic synthesis by enabling the development of efficient and sustainable methodologies for the construction of complex molecules. Its versatility and efficacy make it a valuable reagent for chemists working in the field of chemical synthesis.

Literature

• Synthesis, characterization and anticancer studies of mixed ligand dithiocarbamate palladium(II) complexes.

  European journal of medicinal chemistry 20110901

• Synthesis of InP nanofibers from tri(m-tolyl)phosphine: an alternative route to metal phosphide nanostructures.

  Dalton transactions (Cambridge, England : 2003) 20100107