1092390-02-7 | 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$16.00	$11.00
1g	95%	in stock	$21.00	$15.00
5g	95%	in stock	$69.00	$49.00

Description

• Catalog Number: AB51736
• Chemical Name: 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester
• CAS Number: 1092390-02-7
• Molecular Formula: C22H23BO2
• Molecular Weight: 330.2278
• MDL Number: MFCD09800562
• SMILES: CC1(C)OB(OC1(C)C)c1ccc(cc1)c1ccc2c(c1)cccc2

Upstream Synthesis Route

The 4,4,5,5-tetramethyl-2-(4-naphthalen-2-ylphenyl)-1,3,2-dioxaborolane is a versatile compound widely used in chemical synthesis as a key building block for the creation of complex organic molecules. Its unique structure allows it to participate in a variety of reactions, leading to the formation of various functional groups and stereocenters with high efficiency and selectivity. This boron-containing compound serves as a valuable reagent in cross-coupling reactions, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura coupling, Heck reaction, or Sonogashira reaction. Additionally, its steric and electronic properties make it a valuable tool for the construction of pharmaceutical intermediates, agrochemicals, and materials with tailored properties. Its application in chemical synthesis has significantly advanced the field of organic chemistry by enabling the rapid and efficient assembly of complex molecular structures with a high degree of control and predictability.