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In organosulfur chemistry, a sulfenyl chloride is a functional group with the connectivity R−S−Cl, where R is alkyl or aryl. Sulfenyl chlorides are reactive compounds that behave as sources of RS+. They are used in the formation of RS−N and RS−O bonds. According to IUPAC nomenclature they are named as alkyl thiohypochlorites, i.e. esters of thiohypochlorous acid.

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  • Sulfenylchloride sind eine Stoffgruppe in der organischen Chemie mit der allgemeinen Formel R–S–Cl, genauer sind es Chloride der Sulfensäure (R–S–OH). Trichlormethansulfenylchlorid (Cl3C–S–Cl) und (Cl–CO–S–Cl) sind Beispiele für präparativ eingesetzte Sulfenylchloride. (de)
  • Un cloruro de sulfenilo es un grupo funcional con la conectividad R-S-Cl, donde R es un grupo alquilo o arilo. Los cloruros de sulfenilo son compuestos reactivos, que se comportan como fuentes de RS+. Son usados en la formación de enlaces RS-N y RS-O. (es)
  • In organosulfur chemistry, a sulfenyl chloride is a functional group with the connectivity R−S−Cl, where R is alkyl or aryl. Sulfenyl chlorides are reactive compounds that behave as sources of RS+. They are used in the formation of RS−N and RS−O bonds. According to IUPAC nomenclature they are named as alkyl thiohypochlorites, i.e. esters of thiohypochlorous acid. (en)
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  • Sulfenylchloride sind eine Stoffgruppe in der organischen Chemie mit der allgemeinen Formel R–S–Cl, genauer sind es Chloride der Sulfensäure (R–S–OH). Trichlormethansulfenylchlorid (Cl3C–S–Cl) und (Cl–CO–S–Cl) sind Beispiele für präparativ eingesetzte Sulfenylchloride. (de)
  • Un cloruro de sulfenilo es un grupo funcional con la conectividad R-S-Cl, donde R es un grupo alquilo o arilo. Los cloruros de sulfenilo son compuestos reactivos, que se comportan como fuentes de RS+. Son usados en la formación de enlaces RS-N y RS-O. (es)
  • In organosulfur chemistry, a sulfenyl chloride is a functional group with the connectivity R−S−Cl, where R is alkyl or aryl. Sulfenyl chlorides are reactive compounds that behave as sources of RS+. They are used in the formation of RS−N and RS−O bonds. According to IUPAC nomenclature they are named as alkyl thiohypochlorites, i.e. esters of thiohypochlorous acid. (en)
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  • Sulfenylchloride (de)
  • Cloruro de sulfenilo (es)
  • Sulfenyl chloride (en)
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