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Atomfair 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanol C11H19BN2O3
Description 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanol (CAS: 1040377-08-9) is a highly specialized boronate ester compound with the molecular formula C11H19BN2O3. This chemical features a pyrazole ring functionalized with a 4,4,5,5-tetramethyl-1,3,2-dioxaborolane moiety and an ethanol side chain, making it a versatile intermediate for organic synthesis and pharmaceutical research. Its unique structure enables applications in Suzuki-Miyaura cross-coupling reactions, medicinal chemistry, and as a precursor for boron-containing scaffolds. The compound is supplied as a high-purity solid with rigorous QC validation, ensuring consistency for sensitive research applications. Store under inert conditions to maintain stability.
Description
Description
2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanol (CAS: 1040377-08-9) is a highly specialized boronate ester compound with the molecular formula C11H19BN2O3. This chemical features a pyrazole ring functionalized with a 4,4,5,5-tetramethyl-1,3,2-dioxaborolane moiety and an ethanol side chain, making it a versatile intermediate for organic synthesis and pharmaceutical research. Its unique structure enables applications in Suzuki-Miyaura cross-coupling reactions, medicinal chemistry, and as a precursor for boron-containing scaffolds. The compound is supplied as a high-purity solid with rigorous QC validation, ensuring consistency for sensitive research applications. Store under inert conditions to maintain stability.
- CAS No: 1040377-08-9
- Molecular Formula: C11H19BN2O3
- Molecular Weight: 238.09
- Exact Mass: 238.1488726
- Monoisotopic Mass: 238.1488726
- IUPAC Name: 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazol-1-yl]ethanol
- SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CN(N=C2)CCO
- Synonyms: 1040377-08-9, 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanol, 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazol-1-yl]ethanol, 2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]ethan-1-ol, 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-PYRAZOLE-1-ETHANOL
Application
This compound is widely used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical development. It serves as a protected boronic acid derivative for controlled functionalization in medicinal chemistry. Researchers also employ it in the design of boron-based enzyme inhibitors and PET radiotracer precursors.
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