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Catalog Number:
44554
CAS Number:
142246-48-8
4-Chloro-7-chlorosulfonyl-2,1,3-benzoxadiazole [Réactif fluorescent bifonctionnel]
Purity:
≥ 98 % (HPLC)
Synonym(s):
Chlorure de 4-chloro-2,1,3-benzoxadiazole-7-sulfonyle, 4-Chloro-7-chlorosulfonylbenzofurazane
Hazmat
Documents
$45.00 /250 mg
Taille
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Informations sur le produit
Numéro CAS 
142246-48-8
Formule moléculaire
C6H2Cl2N2O3S
Poids moléculaire 
0
Point de fusion 
85 - 89 °C
Informations générales
Numéro CAS 
142246-48-8
Formule moléculaire
C6H2Cl2N2O3S
Poids moléculaire 
0
Point de fusion 
85 - 89 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

4-Chloro-7-chlorosulfonyl-2,1,3-benzoxadiazole is widely utilized in research focused on:

  • Fluorescent Labeling: This compound serves as a bifunctional fluorescent reagent, allowing researchers to label biomolecules for imaging and tracking in biological studies, enhancing the visualization of cellular processes.
  • Chemical Synthesis: It is used in the synthesis of various organic compounds, particularly in the development of new materials and pharmaceuticals, due to its reactive chlorosulfonyl group that facilitates further chemical modifications.
  • Environmental Monitoring: The compound can be employed in the detection of specific pollutants in environmental samples, aiding in the assessment of water and soil quality, which is crucial for regulatory compliance.
  • Diagnostic Applications: In the medical field, it can be utilized in the development of diagnostic assays, particularly for identifying specific proteins or pathogens, contributing to faster and more accurate disease detection.
  • Research in Material Science: The unique properties of this compound make it valuable in the development of novel materials, such as polymers and coatings, which can have enhanced durability and functionality compared to traditional materials.

Citations