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Catalog Number:
24672
CAS Number:
39181-43-6
5-(4-clorobencil)-1,3,4-tiadiazol-2-amina
Purity:
≥ 96 % (HPLC)
Synonym(s):
5-[(4-clorofenil)metil]-1,3,4-tiadiazol-2-amina
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Product Information

5-(4-Chlorobenzyl)-1,3,4-thiadiazol-2-amine is a versatile compound recognized for its unique structural properties, making it a valuable asset in various research and industrial applications. This thiadiazole derivative is particularly noted for its potential as a building block in the synthesis of agrochemicals and pharmaceuticals, where its chlorobenzyl group enhances biological activity. Researchers have utilized this compound in the development of novel herbicides and fungicides, capitalizing on its efficacy in controlling plant pathogens and pests. Additionally, its role in medicinal chemistry is noteworthy, as it has been explored for its anti-inflammatory and antimicrobial properties, offering promising avenues for drug development.

The compound's stability and reactivity allow for easy incorporation into complex molecular architectures, making it an attractive option for chemists looking to innovate in their formulations. Its distinct characteristics set it apart from similar compounds, providing a competitive edge in both agricultural and pharmaceutical sectors. With ongoing research into its applications, 5-(4-Chlorobenzyl)-1,3,4-thiadiazol-2-amine holds significant potential for advancing product efficacy and safety in various formulations.

Synonyms
5-[(4-clorofenil)metil]-1,3,4-tiadiazol-2-amina
CAS Number
39181-43-6
Purity
≥ 96 % (HPLC)
Molecular Formula
C9H8ClN3S
Molecular Weight
225.7
MDL Number
MFCD00090499
PubChem ID
702289
Melting Point
193-199 ?C
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
5-[(4-clorofenil)metil]-1,3,4-tiadiazol-2-amina
CAS Number
39181-43-6
Purity
≥ 96 % (HPLC)
Molecular Formula
C9H8ClN3S
Molecular Weight
225.7
MDL Number
MFCD00090499
PubChem ID
702289
Melting Point
193-199 ?C
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-(4-Chlorobenzyl)-1,3,4-thiadiazol-2-amine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, helping to create effective herbicides and pesticides that target specific plant pathogens while minimizing environmental impact.
  • Material Science: The compound is explored for its potential in creating novel materials with unique properties, such as enhanced thermal stability and chemical resistance, which can be beneficial in various industrial applications.
  • Biochemical Research: Researchers utilize this compound in studies related to enzyme inhibition and receptor binding, contributing to the understanding of biological processes and the development of new therapeutic strategies.
  • Analytical Chemistry: It is applied in the development of analytical methods for detecting and quantifying thiadiazole derivatives, aiding in quality control and regulatory compliance in various industries.

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