Skip to main content

Ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate

ADVERTISEMENT
Identification
Molecular formula
C10H9ClN2O3S
CAS number
40051-18-5
IUPAC name
ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate
State
State

At room temperature, ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate is usually in a solid state. It can vary from being a fine powder to more defined crystalline forms based on its packing and synthesis conditions.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.15
Boiling point (Celsius)
351.30
Boiling point (Kelvin)
624.45
General information
Molecular weight
274.69g/mol
Molar mass
274.6900g/mol
Density
1.4080g/cm3
Appearence

Ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate appears as a crystalline solid or powder. Its color ranges from off-white to light yellow, depending on the purity and specific sample conditions. The compound is characterized by a distinct aromatic scent due to the presence of the benzothiadiazole moiety.

Comment on solubility

Solubility of Ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate

Ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate, known for its unique structure, showcases a range of solubility properties influenced by its chemical composition.

Key Breakdown of Solubility:

  • Polar vs. Non-polar Solvents: This compound tends to be more soluble in polar solvents due to the presence of polar functional groups.
  • Water Solubility: Generally, it's expected to have limited solubility in water, primarily because of the hydrophobic characteristics associated with the benzothiadiazole moiety.
  • Organic Solvents: It is likely to be soluble in organic solvents such as ethanol, acetone, or dimethyl sulfoxide (DMSO).
  • Influencing Factors: Factors like temperature and pH can significantly impact solubility, potentially enhancing the dissolution of this compound under certain conditions.

To sum up, while Ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate may not readily dissolve in water, it shows a promising solubility profile in various organic solvents, making it versatile for different applications. In the words of chemists, “the solubility of a compound can determine its utility in both practical and theoretical realms."

Interesting facts

Interesting Facts about Ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate

Ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate is a fascinating compound with a range of notable properties and applications. Below are some captivating insights about this unique chemical:

  • Structural Diversity: This compound features a complex structure that includes a benzothiadiazole ring, which is known for its intriguing electronic properties. Such structural motifs are often involved in designing materials for optoelectronic applications.
  • Biological Activity: Compounds containing benzothiadiazole derivatives are frequently investigated for their biological activities, such as antimicrobial and antifungal properties. This raises interesting possibilities for medicinal chemistry and the development of new pharmaceuticals.
  • Applications in Agriculture: The presence of chloro moieties in its structure suggests potential use in pesticides or herbicides, making it a compound of interest in agrochemical research.
  • Synthetic Pathways: The synthesis of this compound often involves innovative synthetic routes, which provide chemistry students and researchers with insight into organic synthesis techniques and the importance of functional groups in reaction mechanisms.
  • Environmental Impact: As with many synthetic organic compounds, understanding the environmental persistence and degradation pathways of ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate is crucial for assessing its ecological footprint.

Overall, ethyl 2-[(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate exemplifies how intricate organic compounds can reveal significant insights into chemical reactivity, potential applications, and environmental considerations. As the field of chemistry evolves, such compounds will continue to be at the forefront of research and innovation.

Synonyms
BRN 1000507
ACETIC ACID, ((4-CHLORO-2,1,3-BENZOTHIADIAZOL-5-YL)OXY)-, ETHYL ESTER
4-Chloro-5-carboxymethoxybenzo-2,1,3-thiadiazole ethyl ester
DTXSID40183381
((4-Chloro-2,1,3-benzothiadiazol-5-yl)oxy)acetic acid ethyl ester
RefChem:315965
DTXCID50105872
29123-12-4
AN-212/12294077
ethyl [(4-chloro-1,2,3-benzothiadiazol-5-yl)oxy]acetate