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AB73077

110231-30-6 | Diphenyl-1-pyrenylphosphine

Packsize Purity Availability Price Discounted Price    Quantity
10mg 95% in stock $23.00 $16.00 -   +
100mg 95% in stock $72.00 $50.00 -   +
250mg 95% in stock $118.00 $82.00 -   +
1g 95% in stock $283.00 $198.00 -   +
5g 95% in stock $985.00 $690.00 -   +
25g 95% in stock $2,873.00 $2,011.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB73077
Chemical Name: Diphenyl-1-pyrenylphosphine
CAS Number: 110231-30-6
Molecular Formula: C28H19P
Molecular Weight: 386.424221
MDL Number: MFCD00278755
SMILES: c1ccc(cc1)P(c1ccc2c3c1ccc1c3c(cc2)ccc1)c1ccccc1

 

Upstream Synthesis Route
  • Diphenyl-1-pyrenylphosphine is a versatile and highly useful compound in chemical synthesis due to its unique properties and reactivity. As a phosphine ligand, it is commonly employed in transition metal-catalyzed reactions, such as cross-coupling reactions and hydrogenation reactions. Its ability to form stable complexes with various metal catalysts enables efficient and selective transformations in organic synthesis.In organometallic chemistry, diphenyl-1-pyrenylphosphine plays a crucial role as a bidentate ligand, facilitating the coordination of transition metals and influencing the reactivity of the metal center. This coordination chemistry allows for control over the regioselectivity and stereoselectivity of the reactions, leading to the formation of complex molecular architectures with high precision.Additionally, diphenyl-1-pyrenylphosphine can also act as a radical scavenger and a stabilizing agent in radical reactions, providing protection against unwanted side reactions and enhancing the overall yield of the desired products. Its ability to participate in electron transfer processes further expands its utility in various synthetic methodologies.Overall, the application of diphenyl-1-pyrenylphosphine in chemical synthesis is diverse and impactful, offering a wide range of possibilities for the design and execution of sophisticated synthetic pathways in both academic research and industrial settings.
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