1073353-81-7 | 4-Methoxy-2-nitrophenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$49.00	$34.00
250mg	95%	in stock	$79.00	$55.00
1g	95%	in stock	$139.00	$97.00
5g	95%	in stock	$535.00	$374.00
10g	95%	in stock	$923.00	$646.00
25g	95%	in stock	$2,002.00	$1,402.00

Description

• Catalog Number: AB67792
• Chemical Name: 4-Methoxy-2-nitrophenylboronic acid, pinacol ester
• CAS Number: 1073353-81-7
• Molecular Formula: C13H18BNO5
• Molecular Weight: 279.0967
• MDL Number: MFCD10699701
• SMILES: COc1ccc(c(c1)[N+](=O)[O-])B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 365
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2

Upstream Synthesis Route

2-(4-Methoxy-2-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a highly versatile and valuable compound in chemical synthesis. This unique reagent serves as a key building block in the development of various organic compounds due to its ability to participate in a range of reactions.One significant application of 2-(4-Methoxy-2-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is in the field of cross-coupling reactions, particularly in Suzuki-Miyaura coupling. This reaction, catalyzed by palladium, allows for the formation of carbon-carbon bonds between aryl or vinyl boronic acids and halides or pseudohalides. The presence of the dioxaborolane moiety in this compound facilitates the transfer of the aryl or vinyl group to the desired organic substrate, leading to the creation of structurally complex molecules.Moreover, 2-(4-Methoxy-2-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is also utilized in the synthesis of pharmaceuticals, agrochemicals, and materials science due to its role as a reliable and efficient coupling partner in diverse synthetic pathways. Its regioselectivity and high functional group tolerance make it a valuable tool for chemists seeking to access novel compounds with specific stereochemical configurations.This compound's unique structure and reactivity profile make it an indispensable reagent in modern organic synthesis, enabling chemists to efficiently construct complex molecules with precision and control.