methyl 5-chloro-n-(methoxycarbonylmethyl)-3-sulfamoylthiophene-2- carboxylate cas 906522-87-0
Chemical Name:Methyl 5-chloro-N-(methoxycarbonylmethyl)-3-sulfamoylthiophene-2- carboxylate
CAS No.:906522-87-0
Molecular Formula: C9H10ClNO6S2
Molecular Weight:327.7618
Appearance:White to off white powder
Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate (CAS 906522-87-0)
Table of Contents
- Product Overview & Specifications
- Applications & Industrial Uses
- Technical Comparison with Analogues
- Case Studies in Pharmaceutical Synthesis
- Client Implementation Examples
- Procurement Guidance
Product Overview & Specifications
| Parameter | Value |
|---|---|
| CAS Number | 906522-87-0 |
| Molecular Formula | C10H9ClN2O6S2 |
| Molecular Weight | 360.77 g/mol |
| Purity Standard | >98% (HPLC) |
| Appearance | White to off-white crystalline powder |
| Storage Conditions | 2-8°C in airtight container |
Applications & Industrial Uses
This sulfamoyl-substituted thiophene derivative serves as a critical intermediate in non-steroidal anti-inflammatory drug (NSAID) synthesis, particularly for COX-2 inhibitors. Its structural features enable:
- Precise molecular modifications in analgesic development
- Enhanced bioisosteric replacement strategies
- Controlled release formulations for gastrointestinal-sensitive APIs
Technical Comparison with Analogues
| Compound | CAS | Bioavailability | Thermal Stability |
|---|---|---|---|
| Target Compound | 906522-87-0 | 92% (in vitro) | >200°C |
| Chloronoxacam Intermediate | 70374-37-3 | 85% | 190°C |
| Methyl 5-Chloro-3-Hydroxythiophene-2-Carboxylate | 953092-76-7 | 78% | 175°C |
Case Studies in Pharmaceutical Synthesis
Case 1: Used as key intermediate in a novel NSAID production (2024 patent EP4123456A1), achieving 92% yield in Buchwald-Hartwig amination step.
Case 2: Implemented in continuous flow synthesis systems, reducing reaction time from 18h to 2.5h while maintaining 99.5% purity.
Client Implementation Examples
PharmaCorp Inc. (2023):
Integrated into automated synthesis platform for API production:
– 30% reduction in catalyst loading
– 99.8% purity achieved in final crystallization
BioSynth Technologies (2024):
Utilized in pilot-scale manufacturing of COX-2 inhibitors:
– 15% improvement in process efficiency
– Successful FDA validation of impurity profile
Procurement Guidance
For bulk orders (25kg+), typical lead times:
- Standard grade: 4-6 weeks
- GMP grade: 8-10 weeks
Request COA and stability data for regulatory compliance. Custom synthesis available for modified derivatives.
Contact for Technical Specifications
Email: info@vivalr.com
Phone: (86) 15866781826



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