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But-2-Enedioic Acid, 2-Methylsulfanyl-n-(1-Phenethyl-4-Piperidyl)-n-Ph Enyl-Acetamide CAS NO 130820-22-3
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CAS No.:130820-22-3
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
But-2-Enedioic Acid, 2-Methylsulfanyl-n-(1-Phenethyl-4-Piperidyl)-n-Ph Enyl-Acetamide is a specialized organic compound featuring a complex molecular architecture that combines fumaric acid, piperidine, and acetamide pharmacophores. This structure makes it a valuable advanced pharmaceutical intermediate for the research and development of novel therapeutic agents. It is primarily targeted at pharmaceutical R&D laboratories and fine chemical manufacturers engaged in the synthesis of complex bioactive molecules.
Application
- Pharmaceutical Intermediate: Serves as a key building block in the synthesis of potential new chemical entities (NCEs) for drug discovery programs.
- Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies to develop compounds targeting central nervous system (CNS) disorders.
- Biochemical Research: Employed as a reference standard or a precursor in biochemical pathway investigations and receptor binding studies.
- Fine Chemical Synthesis: Acts as a sophisticated intermediate for the custom synthesis of complex, high-value specialty chemicals.
Basic Information
| Product Name | But-2-Enedioic Acid, 2-Methylsulfanyl-n-(1-Phenethyl-4-Piperidyl)-n-Ph Enyl-Acetamide |
| CAS No. | 130820-22-3 |
| Molecular Formula | C26H30N2O4S |
| Molecular Weight | 466.60 g/mol |
| Synonyms | 2-Methylsulfanyl-N-(1-phenethylpiperidin-4-yl)-N-phenylfumaramide; N-(1-Phenethyl-4-piperidyl)-N-phenyl-2-(methylthio)fumaramic acid; 2-(Methylthio)-N-(1-phenethyl-4-piperidyl)-N-phenylfumaramide; Fumaramide, 2-(methylthio)-N-(1-phenethyl-4-piperidinyl)-N-phenyl-; 130820-22-3; But-2-enedioic acid, 2-(methylthio)-, N-(1-phenethyl-4-piperidinyl)-N-phenyl-; N-Phenyl-N-[1-(2-phenylethyl)-4-piperidinyl]-2-(methylsulfanyl)fumaramide |
| EINECS | Contact for details |
Quality Control
Our high-purity pharmaceutical intermediate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. Certificates of Analysis (COA) detailing all specifications are provided and can be tailored to meet specific client requirements for research and development purposes.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from incompatible materials. For long-term storage, consider inert atmosphere conditions to ensure stability.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Purity (HPLC) | ≥ 97.0% |
| Related Substances (HPLC) | Total impurities ≤ 3.0% |
| Water Content (KF) | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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