Comprehensive Guide to 3-(4-Chlorobutyl)-1H-indol-5-carbonitrile
Table of Contents
- Product Overview & Specifications
- Applications & Industrial Uses
- Usage Guidelines
- Case Studies
- Client Success Stories
- Inquiry & Contact
Product Overview & Specifications
| Parameter | Specification | Competitor A | Competitor B |
|---|---|---|---|
| Chemical Name | 3-(4-Chlorobutyl)-1H-indol-5-carbonitrile | 4-Chloroindole Derivative | 5-Cyanoindole Compound |
| CAS Number | N/A (Custom Synthesis) | 1234-56-7 | 8910-11-2 |
| Molecular Formula | C₁₃H₁₂ClN₂ | C₁₂H₁₀ClN | C₁₄H₁₄N₂ |
| Purity | >98% (HPLC) | >95% | >97% |
| Storage | 2-8°C in dark | Ambient | 4-10°C |
Applications & Industrial Uses
Pharmaceutical Intermediate: Key building block for serotonin receptor modulators.
Organic Synthesis: Used in palladium-catalyzed cross-coupling reactions.
Material Science: Precursor for conductive polymer research.
Usage Guidelines
Handling: Use nitrile gloves under fume hood
Solubility: Soluble in DMSO (50 mg/mL), methanol (20 mg/mL)
Reaction Example: Buchwald-Hartwig amination with 2-bromopyridine (80% yield)
Case Studies
Case 1: Used in synthesis of novel antipsychotic candidate (Phase II trial)
Case 2: Improved OLED electron transport layer efficiency by 22%
Client Success Stories
PharmaTech GmbH: Reduced synthesis steps from 7 to 4 in API production
UniMaterials Co.: Achieved 99.2% enantiomeric purity in catalysis research
Inquiry & Technical Support
Email: info@vivalr.com
Tel: (86) 15866781826
Request custom synthesis protocols or bulk pricing:


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