?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.