tert-Butyl 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylate
Product Name:tert-Butyl 4-[4-(4
4
5
5-tetramethyl-1
3
2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylate
CAS:877399-74-1
MFC19H32BN3O4
MW:377.29
EINECS:800-459-4
MOL File:877399-74-1.mol
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Product Overview: tert-Butyl 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylate
Table of Contents
- 1. Product Specifications & Comparative Analysis
- 2. Applications & Use Cases
- 3. Industry Case Studies
- 4. Client Success Stories
- 5. Request a Quote or Inquiry
1. Product Specifications & Comparative Analysis
| Parameter | Specification | Competitor A | Competitor B |
|---|---|---|---|
| CAS Number | N/A (custom synthesis) | N/A | N/A |
| Molecular Formula | C20H32BN3O4 | C20H32BN3O4 | C20H32BN3O4 |
| Purity | >97% (HPLC) | >95% | >90% |
| Storage | 2-8°C, dry | Room temperature | 2-8°C |
2. Applications & Use Cases
Key Applications:
- Suzuki-Miyaura Cross-Coupling: Critical boronated intermediate for synthesizing kinase inhibitors.
- Pharmaceutical Intermediates: Used in the development of anticancer and anti-inflammatory drugs.
- PROTAC Molecules: Enables targeted protein degradation in oncology research.
3. Industry Case Studies
Case Study 1: Kinase Inhibitor Optimization
- Challenge: Low yield in coupling reactions due to unstable boronic ester intermediates.
- Solution: Implementation of tert-butyl-protected piperidine-boronate for enhanced stability.
- Result: 40% increase in reaction efficiency and 99% purity in final API.
4. Client Success Stories
Client A: PharmaCorp (USA)
- Project: Development of a third-generation EGFR inhibitor.
- Usage: Served as a key intermediate in the synthesis of the boronate-containing core structure.
- Outcome: Accelerated preclinical timeline by 6 months; IND submitted in 2024.
Client B: BioHealth Innovations (Germany)
- Project: Creation of a BTK-targeting PROTAC molecule.
- Usage: Integrated into the linker region for improved solubility and bioavailability.
- Outcome: Achieved 80% target degradation at 10 nM concentration in vivo.
5. Request a Quote or Inquiry
For pricing, bulk orders, or technical documentation:
- Email: info@vivalr.com
- Phone: (86) 15866781826
Our team provides:
- Custom synthesis up to kilogram scale
- GMP-grade production for clinical trials
- Regulatory support (DMF, CMC documentation)


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