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Catalog Number:
02335
CAS Number:
7669-54-7
Chlorure de 2-nitrobenzènesulfényle
Purity:
≥ 98% (CG)
Synonym(s):
Chlorure d' o -nitrophénylsulfényle
Hazmat
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Informations sur le produit

2-Nitrobenzenesulfenyl chloride is a versatile chemical compound known for its unique properties and applications in various fields. This compound, also recognized as 2-Nitrophenyl thiohypochlorite, is particularly valued in organic synthesis and analytical chemistry. Its ability to act as a chlorinating agent makes it an essential reagent for the introduction of chlorine into organic molecules, facilitating the synthesis of complex chemical structures. Researchers often utilize 2-Nitrobenzenesulfenyl chloride in the development of pharmaceuticals and agrochemicals, where precise modifications of molecular frameworks are crucial.

In addition to its synthetic applications, this compound is also employed in the preparation of sulfenamides and other sulfur-containing compounds, which are important in various industrial processes. Its unique reactivity and selectivity provide significant advantages over similar chlorinating agents, making it a preferred choice for chemists seeking efficiency and effectiveness in their reactions. With its broad range of applications, 2-Nitrobenzenesulfenyl chloride stands out as a valuable tool for researchers and industry professionals alike.

Numéro CAS 
7669-54-7
Formule moléculaire
C6H4ClNO2S
Poids moléculaire 
189.62
Point de fusion 
74 - 77 °C
Informations générales
Numéro CAS 
7669-54-7
Formule moléculaire
C6H4ClNO2S
Poids moléculaire 
189.62
Point de fusion 
74 - 77 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

2-Nitrobenzenesulfenyl chloride is widely utilized in research focused on:

  • Synthesis of Sulfenamides: This compound serves as a key reagent in the preparation of sulfenamides, which are valuable in pharmaceuticals for their antibacterial and antifungal properties.
  • Organic Synthesis: It plays a crucial role in organic synthesis, particularly in the formation of sulfenyl derivatives, which are important intermediates in the production of various organic compounds.
  • Analytical Chemistry: Used as a derivatizing agent, it helps in the analysis of thiols and other sulfur-containing compounds, enhancing the detection and quantification in various samples.
  • Polymer Chemistry: This chemical is applied in the modification of polymers, improving their thermal stability and mechanical properties, which is beneficial in materials science.
  • Research in Environmental Chemistry: It aids in the study of sulfur compounds in environmental samples, contributing to the understanding of pollution and its effects on ecosystems.

Citations