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Atomfair 4H-1-Benzopyran-2-carbonitrile, 3-methyl-4-oxo- C11H7NO2
Description 3-Methyl-4-oxochromene-2-carbonitrile (CAS No. 5464-68-6) is a high-purity organic compound with the molecular formula C11H7NO2. This chromene derivative is characterized by its cyano and oxo functional groups, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a molecular weight of 185.18 g/mol, this compound is supplied as a fine crystalline powder, ensuring optimal solubility and reactivity for laboratory applications. Ideal for researchers in medicinal chemistry, it serves as a precursor for the development of heterocyclic compounds and bioactive molecules. Strict quality control guarantees ??95% purity (HPLC), meeting the rigorous standards of academic and industrial laboratories.
Description
Description
3-Methyl-4-oxochromene-2-carbonitrile (CAS No. 5464-68-6) is a high-purity organic compound with the molecular formula C11H7NO2. This chromene derivative is characterized by its cyano and oxo functional groups, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a molecular weight of 185.18 g/mol, this compound is supplied as a fine crystalline powder, ensuring optimal solubility and reactivity for laboratory applications. Ideal for researchers in medicinal chemistry, it serves as a precursor for the development of heterocyclic compounds and bioactive molecules. Strict quality control guarantees ??95% purity (HPLC), meeting the rigorous standards of academic and industrial laboratories.
- CAS No: 5464-68-6
- Molecular Formula: C11H7NO2
- Molecular Weight: 185.18
- Exact Mass: 185.047678466
- Monoisotopic Mass: 185.047678466
- IUPAC Name: 3-methyl-4-oxochromene-2-carbonitrile
- SMILES: CC1=C(OC2=CC=CC=C2C1=O)C#N
- Synonyms: 4H-1-Benzopyran-2-carbonitrile, 3-methyl-4-oxo-, BRN 1369277, 33544-09-1, 3-Methyl-4-oxo-4H-1-benzopyran-2-carbonitrile, DTXSID50187219
Application
3-Methyl-4-oxochromene-2-carbonitrile is widely utilized as a key building block in the synthesis of chromene-based pharmaceuticals and agrochemicals. Its reactive cyano and carbonyl groups enable facile derivatization for drug discovery, particularly in anticancer and anti-inflammatory agent development. Researchers also employ this compound in material science for designing fluorescent dyes and organic semiconductors due to its conjugated ??-system.
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