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Catalog Number:
19051
CAS Number:
680618-05-7
Chlorure de 2-éthoxy-5-(téréphtalamido)benzène-1-sulfonyle
Purity:
≥ 97 % (HPLC)
Synonym(s):
Chlorure de 5-(4-carbamoyl-benzoylamino)-2-éthoxy-benzènesulfonyle
Documents
$110.70 /100 mg
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Product Information

2-Ethoxy-5-(terephthalamido) benzene-1-sulfonyl chloride is a versatile sulfonyl chloride compound known for its unique reactivity and application potential in various chemical syntheses. This compound serves as an essential intermediate in the production of sulfonamide derivatives, which are widely utilized in pharmaceuticals and agrochemicals. Its ability to introduce sulfonyl groups into organic molecules makes it a valuable reagent in the development of new drugs and crop protection agents.

Researchers and industry professionals appreciate its efficiency in facilitating nucleophilic substitution reactions, allowing for the rapid synthesis of complex molecules. The compound's stability under a range of conditions further enhances its utility in laboratory settings. With its specific structure, 2-Ethoxy-5-(terephthalamido) benzene-1-sulfonyl chloride stands out for its potential to streamline synthetic pathways, making it a preferred choice for those looking to innovate in medicinal chemistry and material science.

Synonyms
Chlorure de 5-(4-carbamoyl-benzoylamino)-2-éthoxy-benzènesulfonyle
CAS Number
680618-05-7
Purity
≥ 97 % (HPLC)
Molecular Formula
C16H15ClN2O5S
Molecular Weight
382.82
MDL Number
MFCD03424964
PubChem ID
53406935
Appearance
Brun foncé uni
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Chlorure de 5-(4-carbamoyl-benzoylamino)-2-éthoxy-benzènesulfonyle
CAS Number
680618-05-7
Purity
≥ 97 % (HPLC)
Molecular Formula
C16H15ClN2O5S
Molecular Weight
382.82
MDL Number
MFCD03424964
PubChem ID
53406935
Appearance
Brun foncé uni
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-Ethoxy-5-(terephthalamido) benzene-1-sulfonyl chloride is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a versatile reagent in the synthesis of sulfonamide derivatives, which are important in developing pharmaceuticals and agrochemicals.
  • Pharmaceutical Development: It is used in the preparation of targeted drug molecules, particularly in the design of anti-cancer and anti-inflammatory agents, enhancing therapeutic efficacy.
  • Material Science: The compound is applied in creating specialty polymers and coatings, providing improved chemical resistance and durability for industrial applications.
  • Bioconjugation: It facilitates the conjugation of biomolecules, aiding in the development of biopharmaceuticals and diagnostic tools, which are crucial for personalized medicine.
  • Research and Development: This chemical is instrumental in academic and industrial research settings, enabling scientists to explore new chemical pathways and develop innovative solutions across various fields.

Citations