1218790-43-2 | 1-(P-Toluenesulfonyl)pyrrole-2-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$118.00	$83.00
5g	96%	in stock	$449.00	$315.00

Description

• Catalog Number: AA54540
• Chemical Name: 1-(P-Toluenesulfonyl)pyrrole-2-boronic acid pinacol ester
• CAS Number: 1218790-43-2
• Molecular Formula: C17H22BNO4S
• Molecular Weight: 347.2369
• MDL Number: MFCD11045475
• SMILES: Cc1ccc(cc1)S(=O)(=O)n1cccc1B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 548
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 24
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3

Upstream Synthesis Route

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrrole is a versatile compound that finds wide application in chemical synthesis. This unique molecule serves as a valuable building block in organic chemistry, particularly in the synthesis of complex molecules and pharmaceutical intermediates. Due to its functional groups and structural features, it can participate in various key synthetic transformations, including cross-coupling reactions, Suzuki-Miyaura coupling, and metal-catalyzed reactions. Moreover, the presence of the dioxaborolane moiety enhances its reactivity and allows for selective functionalization under mild reaction conditions. Chemists often employ 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrrole as a strategic tool in the construction of diverse molecular scaffolds with high efficiency and selectivity. Its utility in the realm of chemical synthesis highlights its significance as a valuable reagent for advancing synthetic methodologies and accessing novel organic compounds.