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Tolimidone

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Identification
Molecular formula
C17H21N3O
CAS number
76144-81-5
IUPAC name
2-[2-[o-tolyl(phenyl)methoxy]ethyl]guanidine
State
State

At room temperature, the compound is typically found in a solid state.

Melting point (Celsius)
104.00
Melting point (Kelvin)
377.15
Boiling point (Celsius)
461.40
Boiling point (Kelvin)
734.60
General information
Molecular weight
269.37g/mol
Molar mass
269.3610g/mol
Density
1.1050g/cm3
Appearence

The compound appears as a white to off-white crystalline powder. It is characterized by its solid form and typical crystalline properties.

Comment on solubility

Solubility of 2-[2-[o-tolyl(phenyl)methoxy]ethyl]guanidine

The compound 2-[2-[o-tolyl(phenyl)methoxy]ethyl]guanidine exhibits a complex solubility behavior that can be influenced by several factors. Understanding its solubility is crucial for applications in pharmaceuticals and chemical formulations.

  • Polarity: This compound contains both polar and non-polar components, which can significantly affect its solubility in various solvents.
  • In polar solvents: It is likely to have limited solubility due to the hydrophobic nature of the o-tolyl and phenyl groups.
  • In non-polar solvents: This compound is expected to show higher solubility owing to the compatibility of its hydrophobic portions with non-polar environments.
  • Temperature effects: As with many organic compounds, solubility may increase with rising temperature, potentially due to enhanced molecular motion.

Overall, the solubility profile of 2-[2-[o-tolyl(phenyl)methoxy]ethyl]guanidine might be best described as moderate in terms of polar solvents while being favorable in non-polar solvents. Further empirical studies are necessary to delineate its solubility more precisely in various solvent systems.

Interesting facts

Interesting Facts about 2-[2-[o-tolyl(phenyl)methoxy]ethyl]guanidine

This fascinating compound, known as 2-[2-[o-tolyl(phenyl)methoxy]ethyl]guanidine, belongs to a class of compounds that exhibit various biological activities, making it significant in medicinal chemistry.

Key Characteristics

  • Biological Activity: It has shown potential in studies related to its role as a pharmacological agent, particularly in the modulation of biological systems.
  • Structure-Activity Relationship: The unique arrangement of the o-tolyl and phenyl groups in its structure enhances its interaction with target receptors, making it a subject of interest for drug development.
  • Research Applications: This compound is often explored in the context of neurological research due to its possible effects on the central nervous system.

Highlighted Elements

Here are a few noteworthy aspects of this compound:

  • Guanidine Moiety: The guanidine functional group is known for its ability to participate in hydrogen bonding, which is crucial for its biological activity.
  • Chirality: The presence of chiral centers may lead to stereoisomers, each having distinct properties and efficacy, adding another layer of complexity to its study.
  • Medicinal Chemistry: It is a prime example of how organic synthesis can lead to compounds that mimic natural structures, opening doors to new therapeutic options.

As researchers continue to investigate compounds like 2-[2-[o-tolyl(phenyl)methoxy]ethyl]guanidine, its potential implications in drug design and therapeutic strategies become increasingly clear. The blend of molecular intricacies and biological significance showcases the exciting world of chemical compounds!