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Methyl N-(thiazolyl-benzimidazolyl)carbamate

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Identification
Molecular formula
C12H10N4O2S
CAS number
7568-85-0
IUPAC name
methyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate
State
State

The compound is a solid at room temperature, often appearing in a stable powdered form. It is typically non-volatile and requires proper handling to maintain its stability under standard laboratory conditions.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.00
Boiling point (Celsius)
289.00
Boiling point (Kelvin)
562.00
General information
Molecular weight
294.30g/mol
Molar mass
294.3300g/mol
Density
1.3200g/cm3
Appearence

The compound appears as a solid with a crystalline structure. The color can vary based on its specific form but often appears as an off-white to light yellow powder. It is typically handled in its powdered form for experimental and industrial purposes.

Comment on solubility

Solubility of Methyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate

The solubility of methyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate is influenced by various factors, including its molecular structure and the presence of functional groups.

Here's a closer look at its solubility characteristics:

  • Solvent Interaction: This compound may exhibit varying solubility in polar and non-polar solvents due to its diverse chemical structure.
  • Hydrogen Bonding: The potential for hydrogen bonding can significantly enhance its solubility in water, although specific solubility data may be limited.
  • pH Sensitivity: The solubility could be influenced by changes in pH, making it more soluble in acidic or basic environments depending on its ionizable groups.
  • Chemical Modification: Substituents on the benzene and thiazole rings may further affect solubility, either enhancing or hindering interaction with solvents.

In summary, while specific solubility values might be scarce, understanding the implications of molecular interactions is key to predicting the solubility of methyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate in various conditions.

Interesting facts

Interesting Facts about Methyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate

Methyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate, a compound with significant biochemical relevance, showcases the intriguing intersections between organic chemistry and pharmacology.

1. Chemical Structure

This compound combines two notable moieties: the thiazole ring and the benzimidazole structure. The presence of these heterocyclic rings contributes to its unique properties.

2. Biological Significance

The structural components of this compound are not just for show. Here are some of its implications in biology:

  • Antimicrobial Activity: Compounds with similar frameworks have been studied for their efficacy against various microbes.
  • Potential Therapeutics: The thiazole and benzimidazole derivatives are known for their potential use in treating diseases such as cancer and parasitic infections.

3. Mechanism of Action

This compound's effectiveness may partially stem from its ability to interfere with biological pathways. It is believed that:

  • It disrupts metabolic processes in target organisms.
  • It may inhibit specific enzymes crucial for survival, making it a vital player in drug development.

4. Synthesis and Development

Speaking of drug development, the synthesis of this compound presents exciting opportunities:

  • Researchers continue to optimize the synthesis process to enhance yield and reduce environmental impact.
  • The ability to modify the structure slightly can lead to compounds with varying pharmacological profiles.

5. Future Prospects

As scientists delve deeper into exploring methyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate, we can anticipate:

  • A rise in studies investigating its use as a selective therapeutic agent.
  • Enhancements in understanding its mechanistic pathways, leading to better drug design.

In conclusion, this compound is more than just a name. Its rich chemical composition and potential biological applications make it an exciting subject of study in the field of medicinal chemistry.

Synonyms
27146-15-2
5-BENZIMIDAZOLECARBAMIC ACID, 2-(4-THIAZOLYL)-, METHYL ESTER
Cambendazole methyl ester
Cambendazole (me)
BRN 1148616
2-(4-Thiazolyl)-5-benzimidazolecarbamic acid methyl ester
SCHEMBL3500748
SCHEMBL3500750
DTXSID10181612