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Dimetacrine

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Identification
Molecular formula
C11H20ClN2O2S
CAS number
47598-69-4
IUPAC name
2-(dimethylamino)ethyl 5-chloro-3-methyl-isothiazole-4-carboxylate
State
State
At room temperature, Dimetacrine is in a solid state, commonly found as a crystalline powder.
Melting point (Celsius)
158.60
Melting point (Kelvin)
431.75
Boiling point (Celsius)
445.80
Boiling point (Kelvin)
718.95
General information
Molecular weight
274.72g/mol
Molar mass
274.7240g/mol
Density
1.2458g/cm3
Appearence

Dimetacrine is typically found in a solid state. It can appear as a crystalline powder.

Comment on solubility

Solubility of 2-(dimethylamino)ethyl 5-chloro-3-methyl-isothiazole-4-carboxylate

The solubility of 2-(dimethylamino)ethyl 5-chloro-3-methyl-isothiazole-4-carboxylate in various solvents is influenced by its unique molecular structure, which contains both hydrophilic and hydrophobic components. This dual nature can be summarized as follows:

  • Hydrophilic Characteristics: The presence of the carboxylate group enhances solubility in polar solvents, such as water and alcohols, due to the ability to form hydrogen bonds.
  • Hydrophobic Characteristics: The isothiazole ring contributes hydrophobic interactions, which can reduce solubility in aqueous environments.

Typically, the solubility behavior can be categorized as:

  1. High Solubility: Generally soluble in polar protic solvents.
  2. Moderate Solubility: Limited solubility in non-polar solvents.

It’s worth noting that the solubility of this compound can be affected by:

  • The temperature of the solvent
  • The pH of the solution
  • Presence of other ions or molecules that can interact with the compound

Overall, understanding the solubility of this compound is crucial for its applications in organic synthesis and biological studies, as stated: "A compound's solubility can often dictate its availability and reactivity in chemical processes."

Interesting facts

Interesting Facts about 2-(Dimethylamino)ethyl 5-chloro-3-methyl-isothiazole-4-carboxylate

2-(Dimethylamino)ethyl 5-chloro-3-methyl-isothiazole-4-carboxylate is a remarkable compound that showcases the fascinating world of organic chemistry. Here are some intriguing facts:

  • Structural Distinction: This compound belongs to the isothiazole class, which is known for its unique ring structure that includes both sulfur and nitrogen atoms. This gives it distinct chemical properties compared to other heterocycles.
  • Biological Activity: Compounds containing the isothiazole ring have demonstrated a variety of biological activities, including potential antibacterial and antifungal properties. Researchers are continually exploring these capabilities for pharmaceutical applications.
  • Versatile Applications: Due to the presence of the dimethylamino group, this compound can interact effectively with biological targets. It is often synthesized as part of drug development, particularly for developing new therapeutic agents in medicinal chemistry.
  • Environmental Relevance: Understanding compounds like this is vital in the context of environmental chemistry, as many isothiazoles have been studied for their effects on living organisms and ecosystems.
  • Storage and Stability: With the right conditions, this compound exhibits good stability, making it a suitable candidate for storage and transport during research and manufacturing processes.

In conclusion, 2-(Dimethylamino)ethyl 5-chloro-3-methyl-isothiazole-4-carboxylate is more than just a chemical; it encapsulates a breadth of scientific inquiry from medicinal chemistry to environmental studies. Its diverse applications and remarkable structural characteristics make it a compound of significant interest in the field of chemistry.

Synonyms
22164-92-7
DTXSID40944813
2-(dimethylamino)ethyl 5-chloro-3-methyl-1,2-thiazole-4-carboxylate
BRN 1110510
RefChem:1061794
5-Chloro-3-methyl-4-isothiazolecarboxylic acid 2-(dimethylamino)ethyl ester
DTXCID401373145
4-ISOTHIAZOLECARBOXYLIC ACID, 5-CHLORO-3-METHYL-, 2-(DIMETHYLAMINO)ETHYL ESTER