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Caramiphen

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Identification
Molecular formula
C22H27NO3
CAS number
77-44-1
IUPAC name
(1-ethyl-3-piperidyl) 2-ethoxy-2,2-diphenyl-acetate
State
State

Caramiphen is a solid at room temperature.

Melting point (Celsius)
170.50
Melting point (Kelvin)
443.65
Boiling point (Celsius)
185.70
Boiling point (Kelvin)
458.85
General information
Molecular weight
377.50g/mol
Molar mass
377.4980g/mol
Density
1.0600g/cm3
Appearence

Caramiphen typically appears as a white or off-white crystalline powder. It is usually odorless or may have a slight characteristic odor. The powder is generally fine and homogeneous.

Comment on solubility

Solubility of (1-ethyl-3-piperidyl) 2-ethoxy-2,2-diphenyl-acetate

The solubility of the compound (1-ethyl-3-piperidyl) 2-ethoxy-2,2-diphenyl-acetate, with the chemical formula C21H25NO3, can be influenced by several factors. Below are key aspects to consider:

  • Polarity: The presence of both alkyl and aromatic groups contributes to a mixed polarity, affecting how it interacts with solvents.
  • Hydrogen Bonding: The nitrogen atom in the piperidine ring may allow for hydrogen bonding with polar solvents, enhancing solubility.
  • Solvent Types: It is likely to be more soluble in organic solvents such as ethanol or dichloromethane than in water due to its hydrophobic characteristics.

In summary, the solubility of this compound is moderate in organic solvents and its solubility can be explained through its structural features, such as:

  1. The ethoxy and diphenyl groups adding to the nonpolar character.
  2. The piperidine component potentially increasing compatibility with polar environments.

As a result, understanding the solubility of (1-ethyl-3-piperidyl) 2-ethoxy-2,2-diphenyl-acetate involves examining both its chemical interactions and the nature of the solvents applied.

Interesting facts

Interesting Facts about (1-Ethyl-3-piperidyl) 2-ethoxy-2,2-diphenyl-acetate

(1-Ethyl-3-piperidyl) 2-ethoxy-2,2-diphenyl-acetate is a fascinating compound, notable for its structural complexity and potential applications. Here are some intriguing points to consider:

  • Structural Insight: This compound showcases a unique arrangement of both piperidine and acetic acid components, which can lead to interesting interactions in biological systems.
  • Pharmaceutical Potential: Given its piperidine structure, scientists are exploring its capacity as a candidate for drug development. Compounds with piperidine rings often exhibit remarkable biological activity.
  • Synthetic Versatility: The diverse functional groups present in this compound allow for various synthetic pathways, making it a useful intermediate in organic chemistry.
  • Chirality: The presence of multiple chiral centers raises the possibility of developing enantiomerically pure forms, which is a critical factor in medicinal chemistry for enhancing drug efficacy and minimizing side effects.
  • Research Focus: Ongoing studies are investigating its properties and interactions, as researchers work to understand how such compounds can be optimized for therapeutic use.
  • Interdisciplinary Relevance: The application of this compound may extend into fields like materials science and nanotechnology, highlighting the interconnectedness of chemistry with other scientific domains.

As a scientist or chemistry student, delving into the properties and possibilities of (1-Ethyl-3-piperidyl) 2-ethoxy-2,2-diphenyl-acetate not only enriches your understanding of organic compounds but also opens up discussions about their impact on future technology and medicine.

In the words of Richard Feynman, "The imagination of nature is greater than the imagination of man." This quote is particularly relevant in the realm of chemical compounds—each one is a testament to nature's creativity and complexity.