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Benzphetamine

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Identification
Molecular formula
C17H21N
CAS number
156-08-1
IUPAC name
3,3-diphenyl-N-(1-phenylethyl)propan-1-amine
State
State

At room temperature, benzphetamine is typically in a solid state, commonly found in the form of a powder for its use as a medication.

Melting point (Celsius)
194.00
Melting point (Kelvin)
467.15
Boiling point (Celsius)
327.50
Boiling point (Kelvin)
600.65
General information
Molecular weight
239.37g/mol
Molar mass
239.3820g/mol
Density
1.0038g/cm3
Appearence

Benzphetamine typically appears as a crystalline powder that is white or off-white in color.

Comment on solubility

Solubility of 3,3-diphenyl-N-(1-phenylethyl)propan-1-amine

The solubility of the compound 3,3-diphenyl-N-(1-phenylethyl)propan-1-amine (C17H21N) in various solvents is notable due to its unique molecular structure. Understanding its solubility can provide valuable insights into its behavior in different chemical environments.

Solubility Characteristics

  • Aromatic Nature: The presence of multiple phenyl groups enhances its hydrophobic character, suggesting limited solubility in water.
  • Solvent Compatibility: It is likely soluble in organic solvents such as ethanol, methanol, and dichloromethane due to its lipophilic nature.
  • Polarity Considerations: The amine group introduces some polarity; however, the overall large non-polar region outweighs this effect.

In summary, while 3,3-diphenyl-N-(1-phenylethyl)propan-1-amine is expected to be poorly soluble in aqueous solutions, it exhibits compatibility with non-polar organic solvents. This characteristic makes it significant in applications involving organic synthesis and drug formulation, where solubility plays a crucial role in efficacy and reactivity.

Interesting facts

Interesting Facts about 3,3-Diphenyl-N-(1-phenylethyl)propan-1-amine

This compound belongs to the class of organic amines and showcases some remarkable properties that intrigue both scientists and students. Here are some points of interest regarding this compound:

  • Structure and Functionality: The presence of two phenyl groups on the amine side chain enhances the compound's stability and interactions with biological systems.
  • Pharmaceutical Applications: Compounds like this one can potentially act as intermediates in the synthesis of pharmaceutical agents, making it a valuable subject of study.
  • Enantioselective Synthesis: The compound's chirality introduces avenues for research in asymmetric synthesis, a critical area in organic chemistry focusing on creating specific enantiomers.
  • Interaction Studies: Its structure allows for insightful studies regarding ligand-receptor interactions, particularly in the context of neurological activity due to its amine group.

As a quote from a renowned chemist states, "The greatest challenge is in understanding how structure dictates function." This compound perfectly exemplifies that principle, bridging structure with potential applications. Furthermore, exploring the reactivity and selectivity of such compounds can lead to significant advancements in drug design and development.

In summary, the study of 3,3-diphenyl-N-(1-phenylethyl)propan-1-amine not only broadens our understanding of organic amines but also opens doors to potentially groundbreaking pharmacological innovations. As research continues, the implications of this compound in both academia and industry remain a captivating focus.

Synonyms
fendiline
13042-18-7
Fendilina
Fendilinum
3,3-diphenyl-N-(1-phenylethyl)propan-1-amine
Fendiline [INN]
Phendilin
Fendilinum [INN-Latin]
Fendilina [INN-Spanish]
EINECS 235-915-6
Fendiline (INN)
UNII-S253D559A8
Phendilin; dl-Fendiline
FENDILINE [MI]
Fendilin
S253D559A8
FENDILINE [WHO-DD]
Benzenepropanamine, gamma-phenyl-N-(1-phenylethyl)-
Benzenepropanamine, .gamma.-phenyl-N-(1-phenylethyl)-
CHEMBL254832
DTXSID5048473
N-(3,3-Diphenylpropyl)-.alpha.-methylbenzylamine
Benzylamine, N-(3,3-diphenylpropyl)-.alpha.-methyl-
N-(3,3-diphenylpropyl)-1-phenylethylamine
Fendilinum (INN-Latin)
N-(1-Phenylethyl)-3,3-diphenylpropylamine
Fendilina (INN-Spanish)
NCGC00018223-06
Celltech Brand of Fendiline Hydrochloride
N-(3,3-Diphenylpropyl)-alpha-methylbenzylamine
SPBio_001131
Spectrum_000443
Prestwick0_000270
Prestwick1_000270
Prestwick2_000270
Prestwick3_000270
Spectrum2_001006
Spectrum3_001436
Spectrum4_000417
Spectrum5_001302
SCHEMBL63814
BSPBio_000120
BSPBio_003172
KBioGR_000714
KBioSS_000923
DivK1c_000604
SPBio_002339
BPBio1_000132
DTXCID1028447
BDBM61401
CHEBI:94434
cid_5702162
HY-B0984A
KBio1_000604
KBio2_000923
KBio2_003491
KBio2_006059
KBio3_002392
NINDS_000604
GLXC-15122
VU717
AKOS022180841
DB08980
IDI1_000604
QTL1_000037
NCGC00018223-02
(3,3-diphenylpropyl)(1-phenylethyl)amine
SBI-0051635.P002
AB00053592
CS-0013595
NS00005501
3,3-Diphenyl-N-(1-phenylethyl)-1-propanamine
D07185
AB00053592_14
3,3-Diphenyl-N-(1-phenylethyl)-1-propanamine #
Q999767
3,3-diphenylpropyl(1-phenylethyl)amine;hydrochloride
Benzylamine, N-(3,3-diphenylpropyl)-alpha-methyl-
BRD-A71033472-003-05-6
BRD-A71033472-003-15-5
BRD-A71033472-003-23-9
3,3-diphenyl-N-(1-phenylethyl)-1-propanamine;hydrochloride
235-915-6