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2-Pyrimidinamine, 4-(4-Fluoro-1-Naphthalenyl)-6-(1-Methylethyl)-, Maleate CAS NO 199864-88-5
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CAS No.:199864-88-5
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
2-Pyrimidinamine, 4-(4-Fluoro-1-Naphthalenyl)-6-(1-Methylethyl)-, Maleate (CAS 199864-88-5) is a high-purity, non-nucleoside reverse transcriptase inhibitor (NNRTI) intermediate of significant pharmaceutical importance. This compound is a critical building block in the synthesis of next-generation antiviral and antiretroviral active pharmaceutical ingredients (APIs). It is essential for research institutions and pharmaceutical manufacturers engaged in the development and production of novel therapeutics targeting viral infections.
Application
- Pharmaceutical Intermediate: A key precursor in the synthesis of advanced non-nucleoside reverse transcriptase inhibitors (NNRTIs) for antiviral drug discovery and manufacturing.
- Antiretroviral API Synthesis: Used in the production chain for active pharmaceutical ingredients targeting HIV and other retroviruses.
- Biochemical Research: Serves as a reference standard and a crucial reagent in virology and medicinal chemistry research programs.
- Process Development: Employed in scaling up and optimizing synthetic routes for new chemical entities (NCEs) in preclinical and clinical development.
- Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production of antiviral drugs.
Basic Information
| Product Name | 2-Pyrimidinamine, 4-(4-Fluoro-1-Naphthalenyl)-6-(1-Methylethyl)-, Maleate |
| CAS No. | 199864-88-5 |
| Molecular Formula | C21H20FN3O4 |
| Molecular Weight | 397.40 g/mol |
| Synonyms | 4-(4-Fluoronaphthalen-1-yl)-6-isopropylpyrimidin-2-amine maleate; 4-(4-Fluoro-1-naphthyl)-6-(1-methylethyl)-2-pyrimidinamine maleate; 4-(4-Fluoronaphthalen-1-yl)-6-(propan-2-yl)pyrimidin-2-amine maleate; 2-Amino-4-(4-fluoro-1-naphthyl)-6-isopropylpyrimidine maleate; NNRTI Intermediate Maleate Salt; CAS 199864-88-5 |
| EINECS | Contact for details |
Quality Control
Our production of this pharmaceutical intermediate adheres to strict quality management systems. Every batch is subjected to comprehensive analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. A detailed Certificate of Analysis (COA) is provided with each shipment, and we support customer audits and regulatory submissions. Specifications can be tailored to meet specific cGMP or research-grade requirements.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (HPLC) | Conforms to reference standard |
| Identification (IR) | Conforms to structure |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% |
| 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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