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Atomfair 2-Ethyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane C8H17BO2

Description 2-Ethyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS No. 82954-89-0) is a high-purity organoboron compound with the molecular formula C8H17BO2. This specialized boronic ester is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its stability and reactivity. The compound features a dioxaborolane ring with ethyl and tetramethyl substitutions, offering excellent solubility in common organic solvents such as THF, DCM, and DMF. Ideal for researchers in pharmaceuticals, materials science, and catalysis, it is supplied in rigorously controlled conditions to ensure optimal performance. Available in various packaging options, this reagent is a critical tool for advanced synthetic applications.

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Description

Description

2-Ethyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS No. 82954-89-0) is a high-purity organoboron compound with the molecular formula C8H17BO2. This specialized boronic ester is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its stability and reactivity. The compound features a dioxaborolane ring with ethyl and tetramethyl substitutions, offering excellent solubility in common organic solvents such as THF, DCM, and DMF. Ideal for researchers in pharmaceuticals, materials science, and catalysis, it is supplied in rigorously controlled conditions to ensure optimal performance. Available in various packaging options, this reagent is a critical tool for advanced synthetic applications.

  • CAS No: 82954-89-0
  • Molecular Formula: C8H17BO2
  • Molecular Weight: 156.03
  • Exact Mass: 156.1321599
  • Monoisotopic Mass: 156.1321599
  • IUPAC Name: 2-ethyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • SMILES: B1(OC(C(O1)(C)C)(C)C)CC
  • Synonyms: 82954-89-0, 2-ethyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, DTXSID50449122, DTXCID20399943, 808-111-3

Application

2-Ethyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is primarily employed as a boronating agent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Its stability under ambient conditions makes it suitable for use in pharmaceutical intermediates and agrochemical synthesis. Researchers also leverage its reactivity in polymer chemistry and materials science for functionalizing organic frameworks.

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