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Butoxyphenylpiperidinopropanone

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Identification
Molecular formula
C18H27NO2
CAS number
953083-92-1
IUPAC name
1-(4-butoxyphenyl)-3-(1-piperidyl)propan-1-one
State
State

At room temperature, Butoxyphenylpiperidinopropanone typically exists in a solid state. It is relatively stable under standard conditions but may degrade or react when exposed to certain environments.

Melting point (Celsius)
102.00
Melting point (Kelvin)
375.15
Boiling point (Celsius)
411.30
Boiling point (Kelvin)
684.40
General information
Molecular weight
291.42g/mol
Molar mass
291.4190g/mol
Density
1.0450g/cm3
Appearence

Butoxyphenylpiperidinopropanone usually appears as a solid crystalline substance. It may have a color ranging from white to off-white or pale yellow. Its texture can vary based on its purity and form.

Comment on solubility

Solubility of 1-(4-butoxyphenyl)-3-(1-piperidyl)propan-1-one (C18H27NO2)

The solubility of 1-(4-butoxyphenyl)-3-(1-piperidyl)propan-1-one is influenced by its molecular structure and functional groups. This compound features a combination of hydrophobic (butoxy and phenyl groups) and polar attributes (piperidyl and carbonyl moieties), which can impact its solubility in various solvents.

Key Aspects of Solubility:

  • Polar Solvents: The presence of the carbonyl group likely enhances the solubility in polar solvents such as methanol or ethanol.
  • Non-Polar Solvents: Conversely, the hydrophobic characteristics of the butoxy and phenyl substitutions may allow the compound to dissolve better in non-polar solvents like hexane or chloroform.
  • Aqueous Solutions: Given its relatively large molecular weight and hydrophobic regions, the solubility in water is expected to be low, which is common for organic compounds with sizable non-polar sections.
  • Temperature Influence: Increased temperature may improve solubility across solvents due to enhanced kinetic activity.

In summary, understanding the solubility profile of 1-(4-butoxyphenyl)-3-(1-piperidyl)propan-1-one is crucial for its application in various chemical and biological systems. It showcases the balance between hydrophilic and hydrophobic interactions, a common theme in organic compound solubility.

Interesting facts

Interesting Facts about 1-(4-butoxyphenyl)-3-(1-piperidyl)propan-1-one

1-(4-butoxyphenyl)-3-(1-piperidyl)propan-1-one is a fascinating compound that showcases the interplay between organic chemistry and medicinal applications. As a member of the class of compounds known as ketones, it possesses unique chemical properties that are of significant interest to scientists and researchers alike.

Key Features:

  • Structural Complexity: This compound features a complex architecture, comprising a butoxy group, a phenyl ring, and a piperidyl moiety. Such structure allows for diverse interactions with biological systems.
  • Potential Applications: Due to its structure, this compound is often explored for its potential therapeutic effects, especially in relation to neurological disorders. It is crucial in drug design and development.
  • Research Interest: Compounds similar to this one have been studied for their affinity to various receptor sites in the brain, enabling advancements in understanding pharmacology and medicinal chemistry.
  • Functional Groups: The presence of both the ketone and the nitrogen-containing piperidine ring highlights the significance of functional groups in determining the reactivity and interaction of the molecule with other substances.

The study of 1-(4-butoxyphenyl)-3-(1-piperidyl)propan-1-one encapsulates the essence of chemistry: the exploration of how molecular structure influences biological function. As noted by researchers, "The complexity of synthetic compounds often correlates with their therapeutic potential." Continued investigations into this compound not only broaden our understanding of its properties but also pave the way for innovations in pharmacotherapy and beyond.

Synonyms
dyclonine
Dyclocaine
586-60-7
Dyclonin
Diclonina
Dyclocainum
Dycloninum
1-(4-butoxyphenyl)-3-(piperidin-1-yl)propan-1-one
Dycloninum [INN-Latin]
Diclonina [INN-Spanish]
4'-Butoxy-3-piperidinopropiophenone
3-Piperidino-4'-butoxypropiophenone
1-Propanone, 1-(4-butoxyphenyl)-3-(1-piperidinyl)-
1-(4-butoxyphenyl)-3-piperidin-1-ylpropan-1-one
1-(4-Butoxyphenyl)-3-(1-piperidinyl)-1-propanone
2-(1-piperidyl)ethyl p-butoxyphenyl ketone
4-butoxy-beta-piperidinopropiophenone
Dyclonine (INN)
BRN 0224037
CHEBI:4724
UNII-078A24Q30O
4-n-butoxy-beta-(1-piperidyl)propiophenone
PROPIOPHENONE, 4'-BUTOXY-3-PIPERIDINO-
078A24Q30O
DTXSID6047864
1-propanone, 1-(4-butoxyphenyl)-3-(1-piperidinyl)
DYCLONINE [INN]
Dycloninum (INN-Latin)
Diclonina (INN-Spanish)
Dyclonine [INN:BAN]
NCGC00016498-01
CAS-536-43-6
1-Propanone,1-(4-butoxyphenyl)-3-(1-piperidinyl)-
Dyclone (Salt/Mix)
Tanaclone (Salt/Mix)
Spectrum_001016
DYCLONINE [MI]
Prestwick0_000264
Prestwick1_000264
Prestwick2_000264
Prestwick3_000264
Spectrum2_001013
Spectrum3_000410
Spectrum4_000529
Spectrum5_000951
DYCLONINE [VANDF]
DYCLONINE [WHO-DD]
SCHEMBL25773
BSPBio_000108
BSPBio_001940
KBioGR_001137
KBioSS_001496
DivK1c_000632
SPBio_001165
SPBio_002327
BPBio1_000120
GTPL7173
CHEMBL1201217
DTXCID6027840
KBio1_000632
KBio2_001496
KBio2_004064
KBio2_006632
KBio3_001160
N01BX02
R02AD04
BZEWSEKUUPWQDQ-UHFFFAOYSA-N
NINDS_000632
EX-A5489
STK524544
AKOS000505031
DB00645
IDI1_000632
NCGC00016498-02
NCGC00016498-03
NCGC00016498-04
NCGC00016498-05
AC-12286
SBI-0051358.P003
AB00053467
NS00010019
C07881
D07881
AB00053467_13
AB00053467_14
EN300-25300221
Q425386
BRD-K72259270-003-05-8
BRD-K72259270-003-15-7
BRD-K72259270-003-23-1
BRD-K72259270-003-24-9
BRD-K72259270-003-25-6
BRD-K72259270-003-26-4
N8R