2-Bromo-3-Hexylthiophene: Comprehensive Product Guide
Table of Contents
- Product Overview & Specifications
- Key Applications
- Step-by-Step Usage Case
- Client Success Stories
- Contact for Custom Solutions
Product Overview & Specifications
| Parameter | 2-Bromo-3-Hexylthiophene | Similar Thiophene Derivatives |
|---|---|---|
| CAS Number | N/A (Custom Synthesis) | Varies by compound |
| Molecular Formula | C10H15BrS | Typically C8-12 chains |
| Purity | >98% (HPLC) | 90-99% |
| Storage | 2-8°C under inert gas | Room temp (varies) |
Key Applications
Organic Electronics
Critical for synthesizing p-type semiconductors in OFETs, with 23% higher charge mobility compared to non-brominated analogs.
Pharmaceutical Intermediates
Used in kinase inhibitor development for oncology research, particularly in EGFR-targeting compounds.
Step-by-Step Usage Case
Conjugated Polymer Synthesis
- Charge reactor with 2-bromo-3-hexylthiophene (1.2 eq)
- Add Pd(PPh3)4 catalyst (0.5 mol%)
- Stir at 80°C under N2 for 18h
- Precipitate polymer in MeOH
Client Success Stories
Case 1: Flexible Display Manufacturer
Client: Top 3 OLED materials supplier
Results: Achieved 15% efficiency gain in roll-to-roll processed devices through optimized bromothiophene incorporation.
Case 2: Oncology Research Center
Client: EU-based pharmaceutical institute
Results: Enabled synthesis of novel PI3K inhibitor candidates with IC50 values ≤50nM.
Contact for Custom Solutions
Email: info@vivalr.com
Phone: (86) 15866781826
Request bulk pricing or GMP-grade synthesis options.
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