Skip to main content

Fentanyl

ADVERTISEMENT
Identification
Molecular formula
C20H25NO
CAS number
992-86-7
IUPAC name
1,1-diphenyl-3-(1-piperidyl)propan-1-ol
State
State

At room temperature, 1,1-diphenyl-3-(1-piperidyl)propan-1-ol exists as a solid.

Melting point (Celsius)
98.50
Melting point (Kelvin)
371.60
Boiling point (Celsius)
405.50
Boiling point (Kelvin)
678.70
General information
Molecular weight
311.42g/mol
Molar mass
311.4520g/mol
Density
1.2500g/cm3
Appearence

1,1-diphenyl-3-(1-piperidyl)propan-1-ol typically appears as a white crystalline powder. The compound may vary slightly in form but is generally consistent in its solid state presentation.

Comment on solubility

Solubility of 1,1-diphenyl-3-(1-piperidyl)propan-1-ol

1,1-diphenyl-3-(1-piperidyl)propan-1-ol, with the chemical formula C20H25NO, presents interesting solubility characteristics.

Its solubility can be characterized by several key factors:

  • Polarity: The presence of the hydroxyl (-OH) group contributes to its polar nature, suggesting it may have moderate solubility in polar solvents.
  • Solvent Interactions: It is likely to be soluble in organic solvents such as methanol and ethanol due to its balanced hydrophilic and hydrophobic components.
  • Limiting Factors: However, the bulky diphenyl groups may hinder solvation, potentially limiting its solubility in less polar solvents.

In summary, the solubility of 1,1-diphenyl-3-(1-piperidyl)propan-1-ol is moderately soluble in polar solvents while showing decreased solubility in non-polar environments, with the solubility influenced significantly by its molecular structure and the interactions with the solvent.

Interesting facts

Interesting Facts about 1,1-Diphenyl-3-(1-piperidyl)propan-1-ol

1,1-Diphenyl-3-(1-piperidyl)propan-1-ol is a fascinating compound that plays a significant role in medicinal chemistry and various biological studies. Below are some intriguing insights about this compound:

  • Structural Diversity: This compound features two distinct phenyl groups and a piperidine ring, showcasing the versatility in its structural composition. This diversity opens avenues for various biological interactions.
  • Research and Applications: Due to its unique structure, 1,1-diphenyl-3-(1-piperidyl)propan-1-ol has been studied for potential use as an antidepressant and antipsychotic agent. Its interactions within the neurotransmitter systems are of particular interest.
  • Synthesis Techniques: The synthesis of this compound often involves complex organic reactions, highlighting the importance of asymmetric synthesis and stereochemistry in creating specific enantiomers that yield the desired therapeutic effects.
  • Biological Significance: Compounds like this that interact with the central nervous system can provide insights into treating neurological disorders. The understanding of such compounds is vital for developing effective psychopharmacological treatments.
  • Analytical Chemistry: Researchers often employ techniques such as NMR spectroscopy and chromatography to analyze the purity and structural characteristics of this compound, showcasing its importance in analytical methods.

The study of 1,1-diphenyl-3-(1-piperidyl)propan-1-ol not only enhances our understanding of chemical interactions but also contributes to the advancement of pharmaceutical developments, making it a compelling subject for any chemist or student in the field.

Synonyms
pridinol
511-45-5
1,1-diphenyl-3-(piperidin-1-yl)propan-1-ol
Nonplesin
Lyseen
Parks
Parks 12
Parks 12 hommel
Pridinolum
Ridinol
Nonpressin (free base)
1,1-Diphenyl-3-(1-piperidyl)-1-propanol
C-238
Pridinol [INN:DCF]
HH 212
Pridinolum [INN-Latin]
1-Piperidinepropanol, alpha,alpha-diphenyl-
3-(N-Piperidyl)-1,1-diphenyl-1-propanol
1,1-Diphenyl-3-piperidino-1-propanol
alpha,alpha-Diphenyl-1-piperidinepropanol
NSC 23016
NSC-23016
238 C
HSDB 2684
UNII-9E75Q6SUUB
EINECS 208-128-0
9E75Q6SUUB
Pridinol (INN)
Benzhydrol, alpha-(2-piperidinoethyl)-
BRN 0252983
DTXSID0045090
CHEBI:75247
1,1-diphenyl-3-piperidin-1-ylpropan-1-ol
PRIDINOL [HSDB]
NSC23016
PRIDINOL [INN]
PRIDINOL [MI]
pridinol monomesylate
PRIDINOL [WHO-DD]
Benzhydrol, .alpha.-(2-piperidinoethyl)-
DTXCID8025090
.alpha.,.alpha.-Diphenyl-1-piperidinepropanol
5-20-02-00247 (Beilstein Handbook Reference)
alpha-(2-piperidinoethyl)benzhydrol
Pridinol (TN)
Pridinolum (INN-Latin)
NSC 23016; NSC 403797; Nonplesin
1,1-Diphenyl-3-(1-piperidinyl)-1-propanol
1-Piperidinepropanol, .alpha.,.alpha.-diphenyl-
n-Propanol, 1,1-diphenyl-3-(piperidin-1-yl)-
1-Piperidinepropanol,.alpha.-diphenyl-
CAS-511-45-5
3-piperidino-1,1-diphenylpropanol
3-piperidinyl-1,1-diphenylpropan-1-ol
pridinolo
Spectrum_001320
3-(N-piperidinyl)-1,1-diphenyl-1-propanol methanesulfonate
Prestwick0_000799
Prestwick1_000799
Prestwick2_000799
Prestwick3_000799
Spectrum2_001985
Spectrum3_001552
Spectrum4_000728
Spectrum5_001069
NCIStruc1_000328
NCIStruc2_000375
BSPBio_000938
BSPBio_003024
KBioGR_000996
KBioSS_001800
DivK1c_000726
SCHEMBL143298
SPBio_002169
SPBio_002877
BPBio1_001032
CHEMBL404215
KBio1_000726
KBio2_001800
KBio2_004368
KBio2_006936
KBio3_002524
M03BX03
NINDS_000726
NCI23016
Tox21_110022
CCG-37974
MFCD00242961
NCGC00013289
NSC403797
AKOS016001547
Tox21_110022_1
3-piperidino-1,1-diphenyl-1-propanol
DB13642
NSC-403797
IDI1_000726
NCGC00013289-01
NCGC00013289-02
NCGC00013289-03
NCGC00013289-04
NCGC00013289-05
NCGC00013289-06
NCGC00013289-07
NCGC00013289-09
NCGC00023906-03
NCGC00023906-04
NCGC00023906-05
AC-24366
NCI60_001871
SY350396
alpha, alpha-Diphenyl-1-piperidinepropanol
SBI-0051765.P002
AB00053638
NS00001644
1,1-Diphenyl-3-piperidin-1-yl-propan-1-ol
D08418
1,1-Diphenyl-3-(1-piperidinyl)-1-propanol #
AB00053638_16
AB00053638_17
AG-680/20240026
Q827515
BRD-K17565903-066-05-8
BRD-K17565903-066-15-7
BRD-K17565903-066-22-3
BRD-K17565903-066-23-1
208-128-0