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Atomfair Methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate C10H19BO4

Description Methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate (CAS No. 1150561-77-5) is a high-purity boronic ester derivative with the molecular formula C10H19BO4. This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its stability and reactivity as a boron-containing intermediate. Its structure features a 4,4,5,5-tetramethyl-1,3,2-dioxaborolane moiety, which enhances its shelf life and handling properties compared to free boronic acids. The methyl ester group further increases its solubility in organic solvents, making it ideal for use in homogeneous catalytic systems. Suitable for researchers and industrial chemists, this product is rigorously tested for purity and consistency, ensuring reliable performance in advanced synthetic…

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Description

Description

Methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate (CAS No. 1150561-77-5) is a high-purity boronic ester derivative with the molecular formula C10H19BO4. This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its stability and reactivity as a boron-containing intermediate. Its structure features a 4,4,5,5-tetramethyl-1,3,2-dioxaborolane moiety, which enhances its shelf life and handling properties compared to free boronic acids. The methyl ester group further increases its solubility in organic solvents, making it ideal for use in homogeneous catalytic systems. Suitable for researchers and industrial chemists, this product is rigorously tested for purity and consistency, ensuring reliable performance in advanced synthetic applications.

  • CAS No: 1150561-77-5
  • Molecular Formula: C10H19BO4
  • Molecular Weight: 214.07
  • Exact Mass: 214.1376392
  • Monoisotopic Mass: 214.1376392
  • IUPAC Name: methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate
  • SMILES: B1(OC(C(O1)(C)C)(C)C)CCC(=O)OC
  • Synonyms: 1150561-77-5, methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate, DTXSID00674907, DTXCID00625656, 853-169-5

Application

Methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate is primarily employed in palladium-catalyzed cross-coupling reactions, such as the Suzuki-Miyaura reaction, to form carbon-carbon bonds in complex organic molecules. Its stability under ambient conditions makes it a preferred reagent for pharmaceutical and agrochemical synthesis. Additionally, it serves as a key intermediate in the preparation of boron-containing polymers and materials science applications. Researchers value this compound for its consistent reactivity and compatibility with a wide range of functional groups.

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