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Identification
Molecular formula
C9H12Cl2N3
CAS number
171496-08-3
IUPAC name
1-(3,4-dichlorophenyl)-2-ethyl-guanidine
State
State

At room temperature, the compound typically exists as a solid due to its relatively high density and melting point.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
234.12g/mol
Molar mass
234.1260g/mol
Density
1.3900g/cm3
Appearence

1-(3,4-dichlorophenyl)-2-ethyl-guanidine generally appears as a solid crystalline substance which may vary in color from white to off-white.

Comment on solubility

Solubility of 1-(3,4-dichlorophenyl)-2-ethyl-guanidine

The solubility of 1-(3,4-dichlorophenyl)-2-ethyl-guanidine can vary based on several factors, including temperature and the solvent utilized. Generally, this compound exhibits moderate solubility in polar solvents due to its functional groups, which can engage in hydrogen bonding.

Key Points on Solubility:

  • Polar Solvents: It tends to dissolve better in water and other polar solvents, making it suitable for applications in aqueous environments.
  • Nonpolar Solvents: In contrast, its solubility in nonpolar solvents may be limited, underscoring its chemical structure which favors polarity.
  • Temperature Impact: Increased temperature often enhances solubility, allowing for greater interaction between the solvent and the solute.
  • Ionic Interactions: The presence of guanidine groups can influence solubility, as they can attract or repel ions, affecting how the compound interacts in various solvent systems.

Overall, understanding the solubility of 1-(3,4-dichlorophenyl)-2-ethyl-guanidine is essential for predicting its behavior in chemical reactions and its efficacy in applications, particularly in biological systems or as a reagent in organic synthesis.

Interesting facts

Interesting Facts about 1-(3,4-Dichlorophenyl)-2-ethyl-guanidine

1-(3,4-dichlorophenyl)-2-ethyl-guanidine is a compound that has garnered attention in the field of medicinal chemistry, especially for its unique pharmacological properties. Below are some interesting insights about this fascinating compound:

  • Pharmacological Role: This compound functions primarily as a selective antagonist for certain types of receptors, making it a subject of interest in drug development, particularly for neurological disorders.
  • Chemical Structure: The 3,4-dichlorophenyl group attached to the guanidine backbone enhances its activity and selectivity, highlighting the importance of structure-activity relationships in medicinal chemistry.
  • Research Significance: Ongoing studies have shown promise in utilizing this compound as part of therapeutic regimens in conditions such as hypertension and other cardiovascular diseases.
  • Toxicological Considerations: Like many chemicals, the safety profile and potential adverse effects of 1-(3,4-dichlorophenyl)-2-ethyl-guanidine are vital areas of research. Understanding its metabolic pathways can disseminate information valuable for regulatory assessments.
  • Synthetic Pathways: The synthesis of this compound involves various methodologies that chemists are keen to optimize, providing avenues for future innovation in synthetic chemistry.

The exploration of 1-(3,4-dichlorophenyl)-2-ethyl-guanidine presents a plethora of opportunities for scientists and researchers alike. It serves as a reminder of how specific modifications to chemical structures can lead to enhanced biological activity and therapeutic potential, embodying the ever-evolving landscape of pharmaceutical chemistry.

Synonyms
Bayer 78658
BAY 78658
17826-33-4
1-(3,4-Dichlorophenyl)-3-ethylguanidine
Guanidine, N-(3,4-dichlorophenyl)-N'-ethyl-
DTXSID90170448
GUANIDINE, 1-(3,4-DICHLOROPHENYL)-3-ETHYL-
DTXCID7092939
Guanidine, N-(3,4-dichlorophenyl)-N'-ethyl-(9CI)
Guanidine, N-(3,4-dichlorophenyl)-N'-ethyl- (9CI)
AKOS011666488