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3-Methyl-1-(3,4-dimethylphenyl)-2-pyrazolin-5-one
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SHIJIAZHUANG DINGMIN PHARMACEUTICAL SCIENCES CO., LTD
3
Years
Basic Info
CAS Number
18048-64-1
Pharmacopoeia
In-house Standards
Grade
Pharmaceutical Grade
Product Keywords
3-Methyl-1-(3,4-dimethylphenyl)-2-pyrazolin-5-one
Is Manufacturer
No
Samples Provided
NO
Product Description
- 英文名称： 3-Methyl-1-(3,4-dimethylphenyl)-2-pyrazolin-5-one
- 别名：
- CAS号： 18048-64-1
- 分子式： C12H14N2O
- 分子量： 202.25
AI Product Description
*The following content is generated by AI and is for reference only.
3-Methyl-1-(3,4-dimethylphenyl)-2-pyrazolin-5-one is a specialized heterocyclic organic compound belonging to the pyrazolone family. With the molecular formula C₁₂H₁₄N₂O and a molecular weight of approximately 202.25 g/mol, this substance features a distinctive pyrazoline ring substituted with a methyl group at position 3 and a dimethylphenyl moiety at position 1. Its chemical structure confers unique reactivity and stability properties, making it valuable in various industrial and research applications. The specific CAS registry number for this compound is 16879-84-8, which serves as its unique identifier in global chemical databases and regulatory frameworks.
This compound is primarily utilized as an intermediate in the synthesis of advanced pharmaceutical agents, particularly those targeting anti-inflammatory, analgesic, or antipyretic activities. Pyrazolone derivatives are historically significant in drug development, often serving as precursors for non-steroidal anti-inflammatory drugs (NSAIDs) or novel therapeutic candidates. Beyond medicine, 3-Methyl-1-(3,4-dimethylphenyl)-2-pyrazolin-5-one finds application in the production of high-performance dyes and pigments. Its conjugated system allows for vibrant coloration and lightfastness, making it suitable for textile coloring, polymer stabilization, and specialty ink formulations. Additionally, researchers employ this molecule in materials science to explore organometallic coordination complexes, where it acts as a ligand to stabilize metal ions for catalytic processes or magnetic material studies.
Safety data indicates that while generally stable under standard conditions, handling requires adherence to laboratory protocols due to potential skin irritation or respiratory sensitivity associated with fine powders. Proper storage involves keeping the substance in a cool, dry environment away from strong oxidizing agents to prevent decomposition. As demand grows for customized functional materials and next-generation therapeutics, derivatives like this one continue to play a pivotal role in bridging fundamental organic chemistry with practical industrial solutions. Researchers must consult detailed safety data sheets before use to ensure compliance with local regulations regarding hazardous substances. Ultimately, this versatile pyrazolone derivative represents a critical building block for innovation across multiple scientific disciplines.
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