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Caramiphen

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Identification
Molecular formula
C21H29NO3
CAS number
77-50-9
IUPAC name
(1-ethyl-3-piperidyl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate
State
State

At room temperature, Caramiphen is in a solid state. Typically, it is observed as a dry powder.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
451.30
Boiling point (Kelvin)
724.45
General information
Molecular weight
351.49g/mol
Molar mass
351.4940g/mol
Density
1.1123g/cm3
Appearence

Caramiphen is typically found as a white crystalline powder. The compound's crystals may exhibit slight translucence, and the powder form tends to be free-flowing and fine. It may not have a significant odor.

Comment on solubility

Solubility of (1-ethyl-3-piperidyl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate

(1-ethyl-3-piperidyl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate is an organic compound whose solubility can be influenced by various factors such as its molecular structure and polarity. Understanding its solubility properties is crucial for applications in pharmaceuticals and chemical formulations.

Key Points on Solubility:

  • Polarity: The presence of hydroxyl (–OH) groups typically increases solubility in polar solvents, whereas the hydrophobic cyclopentyl and phenyl groups may contribute to reduced solubility in water.
  • Solvent Interaction: This compound is likely to be more soluble in organic solvents like ethanol, methanol, or acetone due to its lipophilic character.
  • Temperature Effects: Solubility can be temperature dependent; it is common for organic compounds to exhibit increased solubility at elevated temperatures.
  • Concentration Considerations: At different concentrations, the solubility of this compound may affect its efficacy in solutions, particularly in formulation chemistry.

In conclusion, the solubility of (1-ethyl-3-piperidyl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate is a multifaceted topic that requires consideration of both structural and environmental factors. As noted, it would generally exhibit greater solubility in non-polar organic solvents, and its behavior in aqueous environments could be limited due to its complex structure.

Interesting facts

Interesting Facts about (1-ethyl-3-piperidyl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate

This intriguing organic compound belongs to a class known as esters, which are often noted for their fragrant properties and roles in both synthetic and natural chemistry. Here are some captivating points about this particular compound:

  • Complex Structure: The presence of both a piperidine ring and an ester functional group makes this compound particularly fascinating. Piperidines are cyclic amines that have significant biological activity, frequently serving as building blocks for various pharmaceuticals.
  • Potential Applications: Due to its structural features, this compound could have applications in medicinal chemistry, potentially acting as a precursor for drug synthesis or having biological activity that could be explored further.
  • Flavors and Fragrances: Esters are widely used in the food and fragrance industries. Although this compound’s specific odor profile may not be well-known, the general characteristics of esters often lead to pleasant scents, echoing the fruity notes commonly found in nature.
  • Synthetic Pathways: The synthesis of such esters typically includes reactions like nucleophilic acyl substitution and can involve various intriguing methodologies, making it a subject of interest for synthetic organic chemists.
  • Research Potential: The unique assembly of cyclopentyl and phenyl substituents around the hydroxyacetate moiety opens avenues for research into its reactivity and potential interactions with biological systems.

As a researcher or chemistry student, engaging with compounds like (1-ethyl-3-piperidyl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate not only bridges foundational organic chemistry and advanced materials science but also inspires innovative approaches in the quest for new pharmaceutical entities. Exploration of compounds with complex architectures enhances our understanding of chemical diversity and potential transformative applications.

Synonyms
467-68-5
N-Ethyl-3-piperidyl phenylcyclopentylglycolate
CHEMBL126644
B3B8503HM8
1-ethylpiperidin-3-yl cyclopentyl(hydroxy)phenylacetate
1-Ethyl-3-piperidyl-alpha-cyclopentyl mandelate
Oprea1_301019
UNII-B3B8503HM8
DTXSID00963641
N-Ethyl-3-piperidyl alpha-phenyl-alpha-cyclopentylglycolate
BDBM50225737
Mandelic acid, alpha-cyclopentyl-, 1-ethyl-3-piperidyl ester
N-ETHYL-3-PIPERIDYL .ALPHA.-PHENYL-.ALPHA.-CYCLOPENTYLGLYCOLATE
BENZENEACETIC ACID, .ALPHA.-CYCLOPENTYL-.ALPHA.-HYDROXY-, 1-ETHYL-3-PIPERIDINYL ESTER