1035690-24-4 | 3-Cyclopropoxyphenylboronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$47.00	$33.00
250mg	97%	in stock	$60.00	$42.00
5g	97%	in stock	$712.00	$498.00
10g	97%	in stock	$1,178.00	$824.00
25g	97%	in stock	$2,111.00	$1,478.00

Description

• Catalog Number: AE24304
• Chemical Name: 3-Cyclopropoxyphenylboronic acid pinacol ester
• CAS Number: 1035690-24-4
• Molecular Formula: C15H21BO3
• Molecular Weight: 260.1364400000001
• MDL Number: MFCD16994464
• SMILES: CC1(C)OB(OC1(C)C)c1cccc(c1)OC1CC1

Upstream Synthesis Route

2-(3-Cyclopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile compound widely employed in chemical synthesis processes. This particular boronic ester derivative is highly valued in organic chemistry for its unique reactivity and compatibility with various coupling reactions. One of the key applications of 2-(3-Cyclopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is its role as a valuable building block in Suzuki-Miyaura cross-coupling reactions.In the realm of chemical synthesis, Suzuki-Miyaura cross-coupling is a fundamental method for forming carbon-carbon bonds. By utilizing 2-(3-Cyclopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane as a boronic ester partner in this reaction, chemists can efficiently and selectively construct complex organic molecules with high yields. The strategic incorporation of this compound enables the introduction of the cyclopropoxyphenyl group into target molecules, thereby facilitating the synthesis of diverse pharmaceuticals, agrochemicals, and advanced materials.Moreover, the exceptional stability and tunable reactivity of 2-(3-Cyclopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane make it a valuable tool for synthetic chemists seeking to access novel molecular architectures. By harnessing the unique properties of this compound, researchers can explore innovative synthetic pathways and streamline the preparation of intricate organic compounds with precise control over stereochemistry and functionality.