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Furfenorex

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Identification
Molecular formula
C16H21NO
CAS number
3232-56-8
IUPAC name
N-(2-furylmethyl)-N-methyl-1-phenyl-propan-2-amine
State
State

At room temperature, Furfenorex is in a solid state. It exists as a crystalline powder that is typically stable under normal conditions.

Melting point (Celsius)
46.00
Melting point (Kelvin)
319.15
Boiling point (Celsius)
355.09
Boiling point (Kelvin)
628.24
General information
Molecular weight
263.35g/mol
Molar mass
263.3510g/mol
Density
1.0367g/cm3
Appearence

Furfenorex typically appears as a white or off-white crystalline powder. It is a synthetic compound that may also appear glossy due to its crystal structure.

Comment on solubility

Solubility of N-(2-furylmethyl)-N-methyl-1-phenyl-propan-2-amine

The solubility of N-(2-furylmethyl)-N-methyl-1-phenyl-propan-2-amine, commonly referred to for its complex structure, can vary significantly based on the solvent used. Understanding its solubility is crucial for applications in both synthetic chemistry and pharmacology.

Factors Influencing Solubility

  • Polarity: The presence of polar functional groups in the molecule often enhances solubility in polar solvents.
  • Hydrogen Bonding: Potential for hydrogen bonding with solvents can increase solubility.
  • Temperature: Higher temperatures can generally improve solubility.
  • pH Levels: The ionization state of the compound may influence solubility at different pH levels.

While specific quantitative measurements may not be readily available, it is noted that compounds similar to N-(2-furylmethyl)-N-methyl-1-phenyl-propan-2-amine often show reasonable solubility in organic solvents such as ethanol and dichloromethane. However, their solubility in water can be limited, which poses challenges in formulation and delivery applications.

In conclusion, the solubility properties of this compound warrant careful investigation to optimize its application in various fields. As solubility remains a pivotal aspect in chemical sciences, an understanding of the underlying factors can pave the way for advancements in research and technology.

Interesting facts

Interesting Facts about N-(2-furylmethyl)-N-methyl-1-phenyl-propan-2-amine

N-(2-furylmethyl)-N-methyl-1-phenyl-propan-2-amine, commonly referred to as a derivative of amphetamine, is a fascinating compound with a structure that exhibits unique properties. Here are some interesting aspects of this compound:

  • Chemical Structure: This compound features a furyl group, which contributes to its distinct characteristics. The presence of the aromatic ring enhances its biological activity, making it a subject of interest for pharmacological studies.
  • Pharmacological Potential: Investigations into compounds similar to this one have revealed potential for use in treating conditions such as ADHD and narcolepsy. Its stimulant properties can enhance focus and alertness, leading to a myriad of therapeutic applications.
  • Synthetic Routes: The synthesis of this compound typically involves multi-step organic reactions, showcasing the intricate artistry and precision required in modern organic chemistry. Each step must be carefully controlled to ensure the desired final product.
  • Regulatory Status: Like many derivatives of amphetamine, the regulatory status can vary significantly across different countries. Understanding these regulations is crucial for researchers and pharmaceutical developers.
  • Research Applications: Researchers often use this compound in studying the structure-activity relationship (SAR) of phenethylamines, providing insights into how modifications at various positions can alter biological behavior.

The exploration of N-(2-furylmethyl)-N-methyl-1-phenyl-propan-2-amine opens a pathway to understanding not just this specific compound, but also the broader family of amphetamines. As scientists continue to delve into its properties, they uncover valuable information that could lead to innovative therapeutic strategies and improved understanding of psychoactive substances.

Synonyms
Furfenorex
Frugalan
d-Furfenorex
3776-93-0
Furfenorexum
d-Furfurylmethylamphetamine
X83CZ0Y5TF
(+)-N-Methyl-N-(alpha-methylphenethyl)furfurylamine
FURFENOREX, (+)-
DTXSID1057903
1-Phenyl-2-(N-methyl-N-furfurylamino)propane
SD 27115 FREE BASE
SD-27115 FREE BASE
Furfurylmethylamphetamine d-
DTXCID4031516
223-233-1
dl-Furfenorex
Furfurylmethylamphetamine
13445-60-8
Furfurylmethylamphetamine d-form
N-(furan-2-ylmethyl)-N-methyl-1-phenylpropan-2-amine
554JE75W4N
E-106-E [AS CYCLAMATE]
SD 27115 [AS CYCLAMATE]
2-Furanmethanamine, N-methyl-N-(1-methyl-2-phenylethyl)-
2-Furanmethanamine, N-methyl-N-(1-methyl-2-phenylethyl)-, (+)-
[(furan-2-yl)methyl](methyl)(1-phenylpropan-2-yl)amine
Furfenorex [INN:DCF]
Furfenorexum [INN-Latin]
EINECS 223-233-1
UNII-X83CZ0Y5TF
BRN 4137327
UNII-554JE75W4N
d-N-Methyl N-(phenyl-1 propyl-2) furfurylamine [French]
FURFENOREX [INN]
FURFENOREX [MART.]
DSSTox_CID_31516
DSSTox_RID_97401
d-N-Methyl N-(phenyl-1 propyl-2) furfurylamine
DSSTox_GSID_57727
SCHEMBL164756
CHEMBL2107558
FURFENOREX, (+/-)-
Furfurylamine, N-methyl-N-(alpha-methylphenethyl)-, (+)-
CHEBI:134942
Tox21_113981
FURFURYLMETHYLAMPHETAMINE DL-FORM
NCGC00274278-01
CAS-13445-60-8
FURFURYLMETHYLAMPHETAMINE D-FORM [MI]
NS00030292
FURFURYLMETHYLAMPHETAMINE DL-FORM [MI]
Furfurylamine, N-methyl-N-(alpha-methylphenethyl)-
Q1474922
N-(2-Furylmethyl)-N-methyl-1-phenyl-2-propanamine #
(+)-N-METHYL-N-(.ALPHA.-METHYLPHENETHYL)FURFURYLAMINE
S-(+)-N-METHYL-N-(.ALPHA.-METHYLPHENETHYL)FURFURYLAMINE