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Methenmadinone acetate

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Identification
Molecular formula
C16H28NO2
CAS number
83426-05-3
IUPAC name
N-methyl-N-[(3-methylnorbornan-2-yl)methyl]butanamide
State
State

At room temperature, Methenmadinone acetate is typically a solid.

Melting point (Celsius)
153.50
Melting point (Kelvin)
426.65
Boiling point (Celsius)
318.70
Boiling point (Kelvin)
591.85
General information
Molecular weight
256.41g/mol
Molar mass
256.3750g/mol
Density
0.9453g/cm3
Appearence

This compound is typically a white or nearly white crystalline powder. It is odorless and has a bitter taste.

Comment on solubility

Solubility of N-methyl-N-[(3-methylnorbornan-2-yl)methyl]butanamide

The solubility of the compound N-methyl-N-[(3-methylnorbornan-2-yl)methyl]butanamide can be influenced by several factors, notably its molecular structure and intermolecular interactions. As a tertiary amide, this compound may demonstrate varied solubility characteristics depending on the solvent in which it is placed. Here are some key points to consider:

  • Polarity: The presence of the amide functional group typically enhances solubility in polar solvents, such as water, due to the ability to form hydrogen bonds.
  • Alkyl Groups: The bulky alkyl substituents can increase hydrophobic interactions, which may limit solubility in purely polar solvents.
  • Temperature: Solubility can also significantly change with temperature, frequently increasing as the temperature rises.
  • Concentration: At higher concentrations, solubility might decrease due to the saturating nature of the solution.

In general, while one might expect this compound to have some level of solubility in polar solvents, the overall solubility will depend on the balance of its hydrophobic and hydrophilic characteristics. It is essential to conduct experimental solubility tests in various solvents to obtain precise insights.

Interesting facts

Exploring N-methyl-N-[(3-methylnorbornan-2-yl)methyl]butanamide

N-methyl-N-[(3-methylnorbornan-2-yl)methyl]butanamide, a fascinating compound, showcases the intricate world of amides and their derivatives. This compound is particularly interesting due to its unique structural characteristics, which contribute to its potential applications in various fields.

Key Insights

  • Synthetic Chemistry: The synthesis of N-methyl-N-[(3-methylnorbornan-2-yl)methyl]butanamide highlights essential techniques in organic chemistry, showcasing methods such as alkylation and amide formation, crucial for the development of pharmaceutical compounds.
  • Biological Activity: Many compounds similar to this structure exhibit significant biological activities, including potential analgesic and anti-inflammatory effects, making them valuable in drug discovery.
  • Structure-Activity Relationship (SAR): The presence of the norbornane moiety may influence the compound's interaction with biological targets, underscoring the importance of SAR studies in medicinal chemistry.
  • Chirality: This compound has chiral centers, which could lead to enantiomeric variations that might exhibit different biological properties, further emphasizing the need for careful characterization in research.

“In chemistry, the complexities of a single compound can lead to vast possibilities in application and understanding.”

Researchers continue to explore such compounds not only for their immediate effects but also for how slight modifications in structure can lead to enhanced efficacy or reduced side effects. The ongoing study of N-methyl-N-[(3-methylnorbornan-2-yl)methyl]butanamide exemplifies the larger narrative of chemical innovation and the pursuit of new therapeutic agents.

Synonyms
18966-37-5
BRN 2722423
N-Methyl-N-((3-methyl-2-norbornyl)methyl)butyramide
BUTYRAMIDE, N-METHYL-N-((3-METHYL-2-NORBORNYL)METHYL)-
N-Methyl-N-[(3-methyl-2-norbornyl)methyl]butyramide
N-methyl-N-[(3-methyl-2-bicyclo[2.2.1]heptanyl)methyl]butanamide
DTXSID90940481
N-Methyl-N-[(3-methylbicyclo[2.2.1]heptan-2-yl)methyl]butanamide