1219741-94-2 | 4-(Cyclopropyl)phenylboronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$19.00	$13.00
250mg	95%	in stock	$22.00	$16.00
1g	95%	in stock	$87.00	$61.00
10g	95%	in stock	$851.00	$596.00
25g	95%	in stock	$1,668.00	$1,168.00

Description

• Catalog Number: AA54874
• Chemical Name: 4-(Cyclopropyl)phenylboronic acid pinacol ester
• CAS Number: 1219741-94-2
• Molecular Formula: C15H21BO2
• Molecular Weight: 244.137
• MDL Number: MFCD10698529
• SMILES: CC1(C)OB(OC1(C)C)c1ccc(cc1)C1CC1

Computed Properties

• Complexity: 299
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

2-(4-Cyclopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, often referred to as $name$, is a versatile chemical compound widely used in organic synthesis. This compound serves as a valuable boron-containing building block for the creation of various advanced materials and pharmaceuticals. Its unique structure, featuring a cyclopropyl group and multiple methyl groups attached to boron, imparts distinct reactivity and selectivity in chemical reactions.In chemical synthesis, $name$ plays a crucial role as a reagent for Suzuki-Miyaura cross-coupling reactions. This palladium-catalyzed coupling reaction involves the formation of carbon-carbon bonds by coupling an aryl or vinyl boronic acid with an organic halide or pseudohalide. By incorporating 2-(4-Cyclopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane into the reaction scheme, chemists can selectively introduce the cyclopropylphenyl group into the target molecule, enabling the construction of complex organic frameworks with high efficiency.Moreover, this compound is utilized in the synthesis of functionalized building blocks for drug discovery and material science. The presence of the boron moiety in 2-(4-Cyclopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane facilitates further functionalization through diverse chemical transformations, leading to the generation of structurally diverse molecules with potential biological activities or unique properties.In summary, the application of 2-(4-Cyclopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane in chemical synthesis offers chemists a powerful tool for the strategic construction of complex molecules, enabling the rapid and efficient synthesis of diverse compounds with tailored properties and functionalities.