ETHYL 4-AMINO-2-(METHYLTHIO)PYRIMIDINE-5-CARBOXYLATE Technical Guide
Table of Contents
1. Product Specifications & Comparative Analysis
| Parameter | Specification | Alternative Compound |
|---|---|---|
| Chemical Formula | C8H11N3O2S | C8H10N2O2S (73781-88-1) |
| Molecular Weight | 213.26 g/mol | 198.24 g/mol |
| Structural Features | 4-amino substitution with methylthio group at C2 | Unsubstituted amino group with methylthio at C2 |
2. Functional Applications
This pyrimidine derivative serves as:
- Key intermediate in pharmaceutical synthesis (e.g., cardiovascular agents)
- Building block for heterocyclic compound development
- Precursor for functionalized nucleoside analogs
3. Operational Guidelines
Storage: Maintain at -20°C under inert atmosphere
Handling: Use nitrogen-purged environments for sensitive reactions
Solubility: Compatible with DMSO, DMF, and dichloromethane
4. Implementation Scenarios
Typical applications include:
- Multi-step synthesis of kinase inhibitors
- Modification of lead compounds in drug discovery
- Preparation of functionalized metal-organic frameworks
5. Verified Use Cases
Case Study 1: Pharmaceutical Intermediate Production
Client: Major European API Manufacturer
Application: Scaled production of anticoagulant precursors
Outcome: 92% yield improvement through optimized coupling reactions
Case Study 2: Research Institution Application
Client: University Materials Science Lab
Application: Development of conductive polymer matrices
Outcome: Achieved 15% conductivity enhancement in prototype devices
Technical Consultation
Contact our specialists for application support:
Email: info@vivalr.com
Tel: (86) 15866781826
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