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Carfentrazone

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Identification
Molecular formula
C33H37N3O3
CAS number
0
IUPAC name
2-phenoxyethyl 1-(3-cyano-3,3-diphenyl-propyl)-4-phenyl-piperidine-4-carboxylate
State
State

At room temperature, Carfentrazone is in a solid state. It is stable under normal conditions and does not easily convert into either a liquid or a gas without the application of heat.

Melting point (Celsius)
221.40
Melting point (Kelvin)
494.60
Boiling point (Celsius)
465.50
Boiling point (Kelvin)
738.70
General information
Molecular weight
503.62g/mol
Molar mass
503.6220g/mol
Density
1.1610g/cm3
Appearence

Carfentrazone is typically found as a solid. It is known for its unique crystalline structure and appears as a white powder at room temperature. It is often used in its pure form in laboratory settings for various experiments.

Comment on solubility

Solubility Overview

The solubility of 2-phenoxyethyl 1-(3-cyano-3,3-diphenyl-propyl)-4-phenyl-piperidine-4-carboxylate can be quite complex due to its intricate structure and multiple functional groups. In general, the solubility of organic compounds can be influenced by several factors such as:

  • Polarity: Non-polar compounds tend to dissolve well in non-polar solvents, while polar compounds are more soluble in polar solvents.
  • Hydrogen Bonding: The presence of functional groups capable of forming hydrogen bonds can enhance solubility in water.
  • Temperature: Increased temperature often increases the solubility of solids and liquids, although it can decrease the solubility of gases.

This specific compound, with its diverse aromatic components and a piperidine ring, indicates that it may exhibit limited solubility in water but could potentially dissolve in organic solvents such as:

  • Ethyl acetate
  • Chloroform
  • Methanol

As with many organic compounds, a rule of thumb in solubility is: "Like dissolves like." Therefore, understanding the solvent's nature—polar or non-polar—will greatly aid in predicting the solubility behavior of this compound.

Interesting facts

Interesting Facts about 2-phenoxyethyl 1-(3-cyano-3,3-diphenyl-propyl)-4-phenyl-piperidine-4-carboxylate

2-phenoxyethyl 1-(3-cyano-3,3-diphenyl-propyl)-4-phenyl-piperidine-4-carboxylate is a unique compound that belongs to a class of chemistry known for

  • Its intriguing structural components, which include both aromatic and aliphatic segments that contribute to its chemical behavior.
  • The presence of the piperidine ring, known for its applications in various pharmaceuticals and agricultural products.
  • The incorporation of a cyano group, which enhances the compound's reactivity and potential applications in organic synthesis.

This compound showcases the beauty of structural diversity in organic chemistry. Its design is not only interesting from a theoretical standpoint but also has practical implications. Here are a few significant aspects:

  • Pharmaceutical Potential: Due to the functionalities present, compounds like this one may exhibit noteworthy biological activities, making them candidates for drug development.
  • Synthetic Flexibility: The presence of various functional groups provides chemists with multiple pathways for synthetic modifications, enhancing its utility in research and practical applications.
  • Cyclic Structures in Chemistry: The piperidine ring offers interesting reactivity due to its nitrogen atom, which can easily form interactions with other molecules.

As chemistry continues to evolve, compounds such as 2-phenoxyethyl 1-(3-cyano-3,3-diphenyl-propyl)-4-phenyl-piperidine-4-carboxylate provide rich avenues for exploration. The complexity and potential of this compound encapsulate the essence of synthetic organic chemistry, where every molecule tells a story of innovation and discovery.

Synonyms
FETOXILATE
FETOXYLATE
Fetoxilate [INN:BAN]
fetoxilato
UNII-3791SET69Y
3791SET69Y
FETOXILATE [INN]
FETOXILATE [WHO-DD]
DTXSID10202391
4-Piperidinecarboxylic acid, 1-(3-cyano-3,3-diphenylpropyl)-4-phenyl-, 2-phenoxyethyl ester
2-PHENOXYETHYL 1-(3-CYANO-3,3-DIPHENYLPROPYL)-4-PHENYLISONIPECOTATE
fetoxilatum
RefChem:140352
DTXCID10124882
54063-45-5
1-(3-Cyano-3,3-diphenylpropyl)-4-phenyl-4-piperidinecarboxylic acid 2-phenoxyethyl ester
SCHEMBL1815870
CHEMBL2110871
DB-290671
NS00093629
Q27256662