1-(1-ethoxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole NEW

‌1-(1-Ethoxyethyl)-4-Pyrazoleboronic Acid Pinacol Ester (CAS 1029716-44-6)‌
Google Keywords: 1-(1-Ethoxyethyl)-4-Pyrazoleboronic Acid Pinacol Ester, CAS 1029716-44-6, Suzuki Coupling Reagent, Pharmaceutical Intermediate, Boronic Acid Derivatives

🌟 ‌Product Overview‌

‌1-(1-Ethoxyethyl)-4-Pyrazoleboronic Acid Pinacol Ester‌ (CAS 1029716-44-6) is a specialized boronic ester compound widely used in Suzuki-Miyaura cross-coupling reactions for synthesizing complex organic molecules. It serves as a versatile intermediate in pharmaceutical and agrochemical R&D, enabling precise C-C bond formation.

1. ‌Primary Function‌: Facilitates efficient coupling reactions with high selectivity.

2. ‌Applications‌: Drug discovery, heterocyclic compound synthesis, and material science.

✅ ‌Key Advantages‌

🔹 ‌High Reactivity‌ | Purity ≥98.5% (HPLC/GC verified) | Yield >80% in optimized reactions.
🔹 ‌Stability‌ | Stable under inert conditions (2-year shelf life at -20°C).
🔹 ‌Regulatory Ready‌ | Complies with GMP and ISO 9001 standards for research-grade chemicals.

🧪 ‌Applications‌

• ‌Pharmaceutical Synthesis‌: Key intermediate for APIs in oncology and antiviral therapies.

• ‌Agrochemicals‌: Building block for novel pesticides and herbicides.

• ‌Academic Research‌: Used in catalysis studies and molecular diversity libraries.

📜 ‌Quality Assurance‌

• ‌Testing Methods‌: HPLC, GC, NMR, and FTIR for structural validation.

• ‌Standards‌: Meets USP/EP guidelines for boronic acid derivatives.

📈 ‌Market Trends‌

The global boronic acid derivatives market is expected to grow at ‌7.5% CAGR (2024-2030)‌, driven by demand for targeted drug development and green chemistry innovations. This compound’s role in cross-coupling reactions aligns with trends in precision synthesis and sustainable manufacturing.

Enhance your synthesis workflows with 1-(1-Ethoxyethyl)-4-Pyrazoleboronic Acid Pinacol Ester – reliability, purity, and performance in every batch.