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Iododoxepin

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Identification
Molecular formula
C27H29IN2
CAS number
5807-60-1
IUPAC name
2-benzhydryl-N-[(2-iodophenyl)methyl]quinuclidin-3-amine
State
State

At room temperature, Iododoxepin is in a solid state, typically as a crystalline powder.

Melting point (Celsius)
140.00
Melting point (Kelvin)
413.15
Boiling point (Celsius)
386.30
Boiling point (Kelvin)
659.45
General information
Molecular weight
484.34g/mol
Molar mass
484.3380g/mol
Density
1.4000g/cm3
Appearence

Iododoxepin typically appears as a solid, crystalline powder. It may range in color from white to off-white, depending on its purity and specific form.

Comment on solubility

Solubility of 2-benzhydryl-N-[(2-iodophenyl)methyl]quinuclidin-3-amine

The solubility of a compound often plays a critical role in its potential applications in various fields, including pharmaceuticals and materials science. For the compound 2-benzhydryl-N-[(2-iodophenyl)methyl]quinuclidin-3-amine (C27H29IN2), the solubility profile can be quite intriguing. Generally, compounds with complex structures, particularly those containing aromatic rings and halogens, may exhibit varied solubility behaviors depending on the solvent used.

Factors Influencing Solubility:

  • Polarity: The presence of both non-polar (aromatic rings) and polar (amine groups) elements suggests that this compound may exhibit moderate solubility in both polar and non-polar solvents.
  • Hydrogen Bonding: The amino group can form hydrogen bonds, enhancing solubility in polar solvents such as water and alcohols.
  • Solvent Interactions: Its interaction with solvents like DMSO or DMF may lead to increased solubility due to the capacity of these solvents to stabilize various functional groups present.

It is often noted that “the solubility of a compound is a window into its molecular interactions.” Therefore, understanding how 2-benzhydryl-N-[(2-iodophenyl)methyl]quinuclidin-3-amine interacts with solvents can provide insights not only into its chemical behavior but also into its potential efficacy in applications.

While precise solubility data might require experimental validation, predicting solubility based on molecular features remains a valuable approach in pre-experimental research.

Interesting facts

Interesting Facts about 2-benzhydryl-N-[(2-iodophenyl)methyl]quinuclidin-3-amine

This intriguing compound, 2-benzhydryl-N-[(2-iodophenyl)methyl]quinuclidin-3-amine, is a noteworthy member of the quinuclidine family, which has significant implications in medicinal chemistry and pharmacology. Here are some fascinating insights regarding its structure and potential applications:

  • Structural Complexity: The compound features a quinuclidine core which is often associated with diverse biological activity. This bicyclic structure allows for unique spatial arrangements that can enhance its interaction with biological molecules.
  • Pharmacological Potential: Compounds similar to this one have been studied for their potential in treating various neurological disorders. The inclusion of the iodo-phenyl group may enhance the compound's lipophilicity, possibly improving its ability to traverse the blood-brain barrier.
  • Research Interest: The structural features of 2-benzhydryl-N-[(2-iodophenyl)methyl]quinuclidin-3-amine make it a subject of interest in drug design, aiming to develop new therapies targeting conditions such as schizophrenia or depression.
  • Synthetic Versatility: The synthetic routes to create this compound often involve multi-step reactions, showcasing the challenge and creativity inherent in modern organic synthesis. This makes it a valuable learning tool for students in organic chemistry labs.
  • Isotopic Labeling: The presence of iodine suggests potential applications in radiochemistry, particularly for using isotopes in imaging techniques. This can aid in visualizing biological processes in real time.

In summary, 2-benzhydryl-N-[(2-iodophenyl)methyl]quinuclidin-3-amine exemplifies the complexity and potential of small organic molecules in scientific research. As our understanding of its mechanisms deepens, it may pave the way for new therapeutic strategies in combating challenging neurological conditions. "The magic of chemistry lies not only in the reactions but also in the stories that each compound tells," reflects the ever-curious nature of chemical exploration.

Synonyms
L-703,606 oxalate
L-703 606 OXALATE SALT
Lopac0_000761
SCHEMBL8237780
CHEMBL1527682
CCG-204846
SDCCGSBI-0050739.P002
NCGC00015587-02
NCGC00015587-03
NCGC00015587-04
NCGC00015587-05
NCGC00162244-01
L007728