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363607-69-6
[1,1'-Binaphthalen]-4-ylboronic acid

Catalog#:1P007AKL

CAS:363607-69-6

MDL:MFCD16294426

Molecular Formula:C20H15BO2

Molecular Weight:298.1429

UN Number:

Haz Class:

Packing Group:

Synonyms: [1,1'-Binaphthalen]-4-ylboronic acid; 363607-69-6; AKOS015914957; ZINC169745673; EBD2335011; [1,1\'-Binaphthalen]-4-ylboronic acid; DS-15414; OR360112; AB0064621; AX8212916; TC-133722; 4CH-010482; AK-50359; ST24026025; Z4655; M-8818; 4-(naphthalene-1-yl)-1-naphthalene boronic acid; [4-(naphthalen-1-yl)naphthalen-1-yl]boronic acid; I14-7052; C20H15BO2; 4-(1-Naphthyl)naphthalene-1-boronic acid; CTK8B4424; KS-00000ORY; DTXSID00670207; 1,1'-binaphthyl-4-ylboronic acid; ANW-44977; MFCD16294426;

Keywords: 363607-69-6,MFCD16294426,1P007AKL,[1,1'-Binaphthalen]-4-ylboronic acid,C20H15BO2

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P007AKL 98% 250mg $19.00 $14.00 In Stock USA ADD TO CART BUY NOW
1P007AKL 98% 1g $47.00 $36.00 In Stock USA ADD TO CART BUY NOW

  • [1,1'-Binaphthalen]-4-ylboronic acid, also known as BinapB(OH)2, is a valuable reagent in chemical synthesis, particularly in the field of asymmetric catalysis. This compound serves as a versatile chiral ligand in metal-catalyzed reactions, enabling the stereoselective synthesis of various organic molecules. By forming complexes with metal catalysts, [1,1'-Binaphthalen]-4-ylboronic acid can facilitate a range of transformations, such as asymmetric hydroborations, cross-coupling reactions, and C-H activations. Its unique structure and steric properties make it a powerful tool for controlling the stereochemistry of reactions, leading to the formation of enantiomerically enriched products. Researchers and synthetic chemists often rely on this chiral boronic acid derivative to access chiral building blocks and pharmaceutical intermediates in a controlled and efficient manner.

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