1010840-17-1 | 1,2-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyne

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$164.00	$115.00
1g	98%	in stock	$282.00	$197.00

Description

• Catalog Number: AA04618
• Chemical Name: 1,2-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyne
• CAS Number: 1010840-17-1
• Molecular Formula: C14H24B2O4
• Molecular Weight: 277.9599599999999
• MDL Number: MFCD22666429
• SMILES: CC1(C)OB(OC1(C)C)C#CB1OC(C(O1)(C)C)(C)C

Upstream Synthesis Route

1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyne is a versatile compound widely used in chemical synthesis due to its unique properties. This compound serves as an important building block in organic chemistry, particularly in the formation of carbon-carbon bonds through cross-coupling reactions. It can be employed as a key reagent in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials.One of the main applications of 1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyne is in the Suzuki-Miyaura cross-coupling reaction. This reaction involves the coupling of an aryl halide with an organoboron compound in the presence of a palladium catalyst to form a new carbon-carbon bond. The unique structure of 1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyne allows for efficient and selective cross-coupling reactions, making it a valuable tool for the synthesis of biaryl compounds and other organic molecules.Furthermore, 1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyne exhibits high stability and compatibility with a variety of functional groups, making it a versatile reagent in organic synthesis. Its ease of handling and functional group tolerance make it a preferred choice for chemists working on the synthesis of complex molecular structures.Overall, 1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyne is a valuable compound for chemical synthesis, offering a reliable and efficient method for the construction of diverse organic molecules in the field of organic chemistry.