Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
27909
CAS Number:
50850-93-6
Ester éthylique de l'acide 2-amino-1,3-benzothiazole-6-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
2-amino-benzothiazole-6-carboxylate d'éthyle
Documents
$37.96 /1G
Taille
Request Bulk Quote
Product Information

2-Amino-1,3-benzothiazole-6-carboxylic acid ethyl ester is a versatile compound known for its significant applications in pharmaceuticals and agrochemicals. This compound features a unique benzothiazole structure, which is recognized for its biological activity, making it a valuable building block in the synthesis of various bioactive molecules. Researchers utilize this compound in the development of novel drugs, particularly in the fields of anti-inflammatory and antimicrobial agents. Its ethyl ester form enhances solubility, facilitating easier incorporation into formulations and improving bioavailability.

In addition to its pharmaceutical applications, 2-Amino-1,3-benzothiazole-6-carboxylic acid ethyl ester is also employed in the agrochemical industry, where it serves as an intermediate in the synthesis of herbicides and fungicides. The compound's ability to inhibit specific biological pathways makes it a candidate for developing effective crop protection agents. With its dual functionality in both pharmaceutical and agricultural sectors, this compound stands out for its potential to contribute to advancements in health and agriculture.

Synonyms
2-amino-benzothiazole-6-carboxylate d'éthyle
CAS Number
50850-93-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H10N2O2S
Molecular Weight
222.27
MDL Number
MFCD00102724
PubChem ID
601008
Melting Point
244-250 ?C
Appearance
Aiguilles jaune pâle
Conditions
Conserver à 0-8 °C
General Information
Synonyms
2-amino-benzothiazole-6-carboxylate d'éthyle
CAS Number
50850-93-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H10N2O2S
Molecular Weight
222.27
MDL Number
MFCD00102724
PubChem ID
601008
Melting Point
244-250 ?C
Appearance
Aiguilles jaune pâle
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-Amino-1,3-benzothiazole-6-carboxylic acid ethyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to interact with specific biological pathways.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, acting as a fungicide or herbicide, helping to protect crops from pests and diseases, thereby enhancing agricultural productivity.
  • Material Science: The compound is incorporated into polymers and coatings, improving their thermal stability and mechanical properties, which is beneficial for industries requiring durable materials.
  • Analytical Chemistry: It is employed as a reagent in analytical methods for detecting metal ions, providing a reliable way to assess environmental samples for contamination.
  • Biochemical Research: This compound is utilized in various biochemical assays to study enzyme activity and protein interactions, offering insights into cellular processes and potential therapeutic targets.

Citations