1047636-97-4 | 1-Methyl-1H-1,2,3-triazole-5-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$249.00	$175.00
250mg	96%	in stock	$386.00	$270.00
1g	96%	in stock	$945.00	$661.00
5g	96%	in stock	$2,810.00	$1,967.00
10g	96%	in stock	$4,426.00	$3,098.00

Description

• Catalog Number: AD69865
• Chemical Name: 1-Methyl-1H-1,2,3-triazole-5-boronic acid pinacol ester
• CAS Number: 1047636-97-4
• Molecular Formula: C9H16BN3O2
• Molecular Weight: 209.0532
• MDL Number: MFCD16659791
• SMILES: Cn1nncc1B1OC(C(O1)(C)C)(C)C

Upstream Synthesis Route

1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-1,2,3-triazole is a versatile compound commonly used in chemical synthesis as a key building block. Its unique structure enables it to participate in a variety of reactions, making it valuable in the creation of complex organic molecules. In particular, this compound is frequently employed as a ligand in transition metal-catalyzed cross-coupling reactions.Its boron-containing moiety enhances its reactivity and selectivity in various transformations, such as Suzuki-Miyaura coupling, Sonogashira coupling, and Heck reactions. The ability of 1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-1,2,3-triazole to form stable complexes with transition metals allows for efficient carbon-carbon and carbon-heteroatom bond formations in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, this compound has found application in bioconjugation chemistry, enabling the selective modification of biomolecules for research and therapeutic purposes. Its ease of functionalization and compatibility with diverse reaction conditions make it a valuable tool for organic chemists seeking to streamline synthetic pathways and access novel molecular architectures with high efficiency and precision.