N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide

Identification

Molecular formula

C₁₄H₁₇NO₃

CAS number

IUPAC name

N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide

State

The compound is a crystalline solid at room temperature.

Melting point (Celsius)

78.00

Melting point (Kelvin)

351.15

Boiling point (Celsius)

385.00

Boiling point (Kelvin)

658.15

General information

Molecular weight

249.31g/mol

Molar mass

249.3060g/mol

Density

1.1034g/cm³

Appearence

N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide typically presents itself as a white to off-white crystalline powder.

Comment on solubility

Solubility of N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide

N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide is a compound that exhibits interesting characteristics regarding its solubility. Here are key points to consider:

Solvent Compatibility: This compound is likely to be more soluble in organic solvents such as ethanol, methanol, and dichloromethane due to its hydrophobic components.
Polarity Influences: The presence of methoxy groups may enhance solubility in polar solvents to some degree, but the overall molecular structure leans towards a nonpolar behavior.
Water Solubility: Given its organic nature, one should expect low solubility in water. This characteristic is common among many similar compounds.
Temperature Effects: Like many organic compounds, solubility can increase with temperature; thus, heating may facilitate dissolution.

In summary, while N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide may exhibit some solubility in polar solvents, it generally favors nonpolar environments. As stated, "the devil is in the details," and understanding the solubility profile of such compounds is crucial in applications ranging from pharmaceuticals to chemical synthesis.

Interesting facts

Interesting Facts about N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide

N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide is a fascinating compound that has garnered attention in various fields of research due to its unique structure and potential applications. Here are some intriguing insights:

Structural Features: The compound features a prop-2-enamide backbone that is substituted with an allyl group, and a 3,4-dimethoxyphenyl moiety, which imparts significant electron-donating properties. This specific configuration contributes to its reactivity and interaction with biological targets.
Biological Activity: Preliminary studies suggest that compounds similar to N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide may exhibit promising anti-inflammatory and anticancer activities. Such properties make it a candidate for further pharmacological investigations.
Synthetic Route: The synthesis of this compound typically involves a series of reactions including Michael addition and condensation reactions, showcasing the versatility of organic synthesis techniques in generating complex molecules.
Natural Product Inspired: The structure bears resemblance to various natural products known for their biological efficacy. This linkage highlights the importance of studying synthetic derivatives to potentially enhance their therapeutic potential.
Organoleptic Properties: The presence of the methoxy groups can significantly influence the compound’s interaction with taste and olfactory receptors, which is an interesting avenue for sensory science research.

The exploration of N-allyl-3-(3,4-dimethoxyphenyl)prop-2-enamide illustrates how organic compounds can be at the intersection of chemistry, biology, and pharmacology. As ongoing research unfolds, this compound may help unlock new avenues in drug discovery and development.

Synonyms

CBMicro_030264

DivK1c_005640

SCHEMBL8015833

CDS1_004600