115826-95-4 | [(R)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl]palladium(II) chloride

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$13.00	$9.00
250mg	98%	in stock	$16.00	$11.00
1g	95%	in stock	$30.00	$21.00
5g	95%	in stock	$143.00	$101.00

Description

• Catalog Number: AB56259
• Chemical Name: [(R)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl]palladium(II) chloride
• CAS Number: 115826-95-4
• Molecular Formula: C44H32Cl2P2Pd
• Molecular Weight: 799.9984
• MDL Number: MFCD00075254
• SMILES: Cl[Pd-2]1(Cl)[P+](c2ccccc2)(c2ccccc2)c2ccc3c(c2c2c([P+]1(c1ccccc1)c1ccccc1)ccc1c2cccc1)cccc3

Upstream Synthesis Route

[(R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl]palladium(II) chloride, commonly referred to as $name$, is a versatile catalyst widely used in chemical synthesis. This compound plays a crucial role in catalyzing a variety of organic transformations, particularly in the field of asymmetric synthesis.$name$ has been utilized in the preparation of various chiral molecules with high enantioselectivity, making it a valuable tool for the production of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to facilitate asymmetric reactions has led to significant advancements in the development of new synthetic methodologies.One prominent application of $name$ is in cross-coupling reactions, where it promotes the formation of carbon-carbon and carbon-heteroatom bonds with excellent stereochemical control. This catalyst is known for its efficiency in promoting challenging transformations, enabling chemists to access complex molecular structures with high levels of stereoselectivity.Moreover, $name$ has found use in the construction of biologically active compounds and natural products, highlighting its importance in drug discovery and development. Its ability to catalyze reactions under mild conditions and with high efficiency has made it a valuable component in the toolbox of synthetic chemists striving to access optically pure compounds.In summary, $name$ is a powerful catalyst that plays a pivotal role in organic synthesis, particularly in the creation of chiral molecules with precise stereochemistry. Its unique properties make it an indispensable tool for researchers seeking to access enantiomerically enriched compounds in a sustainable and efficient manner.