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Atomfair 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline C12H18BNO2

Description 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (CAS No. 1439929-51-7) is a high-purity boronic ester derivative with the molecular formula C12H18BNO2. This compound features a stable dioxaborolane ring and an aniline moiety, making it a versatile intermediate for Suzuki-Miyaura cross-coupling reactions and other organoboron transformations. Ideal for pharmaceutical, agrochemical, and materials science research, this reagent is rigorously tested for quality, ensuring consistent performance in synthetic applications. Supplied as a crystalline solid with ??95% purity, it is packaged under inert conditions to maintain stability. Store in a cool, dry place away from moisture and oxidizing agents.

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Description

Description

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (CAS No. 1439929-51-7) is a high-purity boronic ester derivative with the molecular formula C12H18BNO2. This compound features a stable dioxaborolane ring and an aniline moiety, making it a versatile intermediate for Suzuki-Miyaura cross-coupling reactions and other organoboron transformations. Ideal for pharmaceutical, agrochemical, and materials science research, this reagent is rigorously tested for quality, ensuring consistent performance in synthetic applications. Supplied as a crystalline solid with ??95% purity, it is packaged under inert conditions to maintain stability. Store in a cool, dry place away from moisture and oxidizing agents.

  • CAS No: 1439929-51-7
  • Molecular Formula: C12H18BNO2
  • Molecular Weight: 219.09
  • Exact Mass: 219.1430590
  • Monoisotopic Mass: 219.1430590
  • IUPAC Name: 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
  • SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=CC=C2N
  • Synonyms: 191171-55-8, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, DTXSID50370422, DTXCID30321457, 626-344-7

Application

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is widely used as a key building block in palladium-catalyzed cross-coupling reactions for the synthesis of biaryl compounds. Its boronate ester group enables efficient aryl-aryl bond formation in medicinal chemistry and materials science. Researchers also employ it in the development of fluorescent probes and polymer precursors due to its reactive aniline group.

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