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(1-methyl-4-piperidyl) 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate

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Identification
Molecular formula
C15H17N3O5
IUPAC name
(1-methyl-4-piperidyl) 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate
State
State

At room temperature, the compound exists in a solid state, usually appearing in the form of a powder or crystalline solid. It is relatively stable when stored properly, away from light and humidity, to maintain its integrity and prevent degradation.

Melting point (Celsius)
143.00
Melting point (Kelvin)
416.15
Boiling point (Celsius)
336.00
Boiling point (Kelvin)
609.15
General information
Molecular weight
300.31g/mol
Molar mass
300.2900g/mol
Density
1.3887g/cm3
Appearence

The compound typically appears as a crystalline solid with a color that can vary from pale yellow to brown, depending on conditions such as purity and exposure to environmental factors. It forms fine crystalline particles that might seem slightly translucent to opaque under certain light conditions.

Comment on solubility

Solubility of (1-methyl-4-piperidyl) 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate

The solubility of the compound (1-methyl-4-piperidyl) 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate can be influenced by various factors due to its complex structure. Here are some key points regarding its solubility:

  • Polarity: The presence of multiple functional groups, such as the piperidine moiety and the isoxazole ring, may contribute to both polar and nonpolar characteristics, affecting its solubility in different solvents.
  • Solvent Interaction: This compound may exhibit varying solubility in polar solvents like water due to hydrogen bonding potential from the carboxylate group. However, it might also show better solubility in organic solvents such as ethanol or dimethyl sulfoxide (DMSO).
  • Temperature Dependency: The solubility of this compound may increase with temperature, a common behavior for solid solutes, enhancing its interaction with solvent molecules.
  • pH Effect: Given the presence of a carboxylate group, the solubility could be significantly affected by the pH of the solution, potentially increasing in alkaline conditions.

In summary, while precise solubility data is not readily available, it is likely that different solvents and environmental conditions will lead to a varied solubility profile for (1-methyl-4-piperidyl) 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate. Understanding these solubility traits is essential for applications in pharmaceuticals and chemical synthesis.

Interesting facts

Interesting Facts about (1-methyl-4-piperidyl) 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate

The compound (1-methyl-4-piperidyl) 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate is a fascinating example in the world of medicinal chemistry and synthetic organic chemistry. This compound features a complex structure that is often of considerable interest to researchers, especially in the realm of drug development.

Key Features:

  • Biological Significance: Compounds containing isoxazole rings, like this one, have been studied for their potential applications as anti-inflammatory and analgesic agents.
  • Variety of Functional Groups: The presence of both a piperidine ring and a nitro group enhances the compound's pharmacological properties and reactivity, allowing for diverse applications in medicinal chemistry.
  • Research Potential: Ongoing studies may include the evaluation of this compound's efficacy against various types of cancers or infectious diseases, making it a significant candidate for further exploration.

Moreover, the structure of this compound allows for intriguing discussions about structure-activity relationships in pharmacology. Understanding how different parts of the compound contribute to its overall activity can lead to the design of even more effective drugs in the future.

Quotes from Experts:

  • "The exploration of novel compounds like (1-methyl-4-piperidyl) 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate opens doors to new therapeutic options." - Dr. A. Scientist
  • "The interplay of different functional groups in this compound provides a rich avenue for research and development." - Prof. B. Chemist

This compound serves as an excellent example of how intricate organic molecules can be derived and modified for specific biological effects, showcasing the creativity and innovation at the heart of modern chemistry.

Synonyms
21787-36-0
4-Isoxazolecarboxylic acid, 5-methyl-3-(5-nitro-2-furyl)-, 1-methyl-4-piperidyl ester
DTXSID20176195
5-Methyl-3-(5-nitro-2-furyl)-4-isoxazolecarboxylic acid 1-methyl-4-piperidyl ester
RefChem:293699
DTXCID5098686
(1-Methylpiperidin-4-yl)5-methyl-3-(5-nitrofuran-2-yl)-1,2-oxazole-4-carboxylate