CAS 147356-78-3
:Cyclopropanecarboxamide, N-methoxy-N-methyl-
Description:
Cyclopropanecarboxamide, N-methoxy-N-methyl- is a chemical compound characterized by its unique cyclopropane ring structure, which contributes to its distinct reactivity and properties. The presence of the carboxamide functional group indicates that it can participate in hydrogen bonding, influencing its solubility and boiling point. The N-methoxy and N-methyl substituents enhance its steric and electronic properties, potentially affecting its interaction with biological targets or other chemical species. This compound may exhibit moderate polarity due to the presence of the methoxy group, which can also influence its solubility in various solvents. Additionally, the cyclopropane moiety may impart strain, leading to increased reactivity compared to more stable cyclic structures. Overall, Cyclopropanecarboxamide, N-methoxy-N-methyl- is of interest in synthetic chemistry and may have applications in pharmaceuticals or agrochemicals, although specific biological activities or applications would require further investigation.
Formula:C6H11NO2
Synonyms:- N-Methoxy-N-methyl-cyclopropanecarboxamide
- N-Methoxy-N-Methylcyclopropanecarboxamide
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Found 4 products.
N-Methoxy-N-methylcyclopropanecarboxamide
CAS:Purity:95.0%Color and Shape:Liquid, No data available.Molecular weight:129.15899658203125Cyclopropanecarboxamide, N-methoxy-N-methyl-
CAS:Formula:C6H11NO2Purity:97%Color and Shape:LiquidMolecular weight:129.1570N-Methoxy-N-methylcyclopropanecarboxamide
CAS:<p>N-Methoxy-N-methylcyclopropanecarboxamide</p>Purity:98%Molecular weight:129.16g/molN-Methoxy-N-methylcyclopropanecarboxamide
CAS:<p>N-Methoxy-N-methylcyclopropanecarboxamide is a selective inhibitor of the enzyme azaindole synthase. This drug was shown to be efficacious in vivo in rats with an azaindole-resistant strain of neutrophil leukemia. It also showed efficacy in vitro against human neutrophils and erythrocytes, as well as human blood cells. Azaindole synthase is an enzyme that catalyzes the synthesis of azaindoles from indole and acetaldehyde. This compound has been identified as a lead optimization candidate for treatment of certain cancers, such as leukemia and lymphoma.</p>Formula:C6H11NO2Purity:Min. 95%Molecular weight:129.16 g/mol



