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4-Ethyl-α-methylamino-3,4-dihydro-2H-pyran-5-carboximidamide

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Identification
Molecular formula
C15H23NO
CAS number
835925-85-6
IUPAC name
1-(4-ethylphenyl)-2-methyl-3-(1-piperidyl)propan-1-one
State
State

At room temperature, this compound is typically found as a solid.

Melting point (Celsius)
180.50
Melting point (Kelvin)
453.65
Boiling point (Celsius)
327.10
Boiling point (Kelvin)
600.25
General information
Molecular weight
231.36g/mol
Molar mass
231.3310g/mol
Density
1.0293g/cm3
Appearence

The compound is usually found as a crystalline powder, ranging from white to off-white in color. It is often finely granular in texture, making it easy to handle in laboratory settings.

Comment on solubility

Solubility of 1-(4-ethylphenyl)-2-methyl-3-(1-piperidyl)propan-1-one (C15H23NO)

The solubility of 1-(4-ethylphenyl)-2-methyl-3-(1-piperidyl)propan-1-one can be characterized by several important aspects:

  • Nature of the Compound: This compound contains both hydrophobic (alkyl and phenyl groups) and polar (piperidyl and carbonyl functional groups) structures, suggesting that its solubility will vary significantly in different solvents.
  • Solvent Compatibility: Typically, such organic compounds are better soluble in organic solvents like:
    • Ethyl acetate
    • Toluene
    • Dichloromethane
    • Alcohols, such as ethanol
  • Water Solubility: Given the structure, the solubility in water is likely to be low due to the large hydrophobic regions that outweigh the polar elements.

As a guiding principle, compounds with significant hydrophobic characteristics tend to show limited solubility in polar solvents. In contrast, they dissolve readily in less polar or non-polar environments. Therefore, it is crucial to conduct solubility experiments in various solvents to ascertain specific solubility rates.

In summary, when considering the solubility of 1-(4-ethylphenyl)-2-methyl-3-(1-piperidyl)propan-1-one, one must evaluate:

  1. The type of solvent being used
  2. The compound’s polar and non-polar functional groups
  3. Temperature, as it often influences solubility

This understanding can guide practical applications and chemical reactions involving this compound.

Interesting facts

Exploring 1-(4-Ethylphenyl)-2-methyl-3-(1-piperidyl)propan-1-one

1-(4-Ethylphenyl)-2-methyl-3-(1-piperidyl)propan-1-one, often referred to as a novel compound in the realm of organic chemistry, has piqued the interest of researchers for several reasons. This compound is notable for its structure and potential applications:

  • Complex Structure: The compound features a piperidine ring, which is common in many pharmaceutical agents, providing a unique interaction profile in biological systems.
  • Potential Pharmacological Interests: Compounds of this class are being investigated for their effects on neurotransmitter systems, particularly in the development of new medications aimed at treating various psychological disorders.
  • Unique Substituents: The presence of both a 4-ethylphenyl group and a methyl group adds to its structural diversity, which can affect its reactivity and interaction with other chemical entities.
  • Applications in Research: Its unique properties make it a candidate for studies related to drug design and synthesis, opening pathways for innovative treatments.
  • Synthetic Pathways: The methods by which this compound can be synthesized may reveal new strategies in organic synthesis, contributing to advancements in the field.

In the words of famous chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” This compound exemplifies this sentiment, as ongoing studies and explorations continue to uncover its potential applications and effects, highlighting the need for further research and experimentation.

As our understanding of such complex compounds evolves, the importance of interdisciplinary collaboration in chemistry, pharmacology, and materials science becomes ever more critical. The exploration of 1-(4-ethylphenyl)-2-methyl-3-(1-piperidyl)propan-1-one will likely contribute to significant breakthroughs in drug development and organic synthesis.

Synonyms
eperisone
64840-90-0
Eperisone [INN]
1-(4-ethylphenyl)-2-methyl-3-(piperidin-1-yl)propan-1-one
Eperisona
(+-)-Eperisone
Eperisonum
Eperisonum [INN-Latin]
Eperisona [INN-Spanish]
4'-Ethyl-2-methyl-3-piperidinopropiophenone
1-(4-ethylphenyl)-2-methyl-3-piperidin-1-ylpropan-1-one
Eperisone (INN)
BRN 1246496
EPERISONE [JAN]
EPERISONE [MI]
1-(4-Ethylphenyl)-2-methyl-3-(1-piperidinyl)-1-propanone
2M2P0551D3
EPERISONE [WHO-DD]
DTXSID5040671
CHEBI:77070
1-Propanone, 1-(4-ethylphenyl)-2-methyl-3-(1-piperidinyl)-
Eperisonum (INN-Latin)
Eperisona (INN-Spanish)
C17H25NO
(2RS)-1-(4-ethylphenyl)-2-methyl-3-(1-piperidyl)propan-1-one
NCGC00167973-01
(4'-ethyl-2-methyl-3-piperidino)propiophenone
UNII-2M2P0551D3
1-Propanone, 1-(4-ethylphenyl)-2-methyl-3-(1-piperidinyl)-, hydrochloride
4-EMPP
E-0646
SCHEMBL194769
CHEMBL1902981
DTXCID3020671
CHEBI:77069
M03BX09
AKOS015960753
DB08992
AC-12144
DB-054734
HY-128891
CS-0101898
D07898
Q426401
BRD-A04252265-001-01-8
BRD-A04252265-003-01-4
rac-1-(4-ethylphenyl)-2-methyl-3-(piperidin-1-yl)propan-1-one