CAS 13165-68-9
:4-Chloro-N-sulfinylbenzenamine
Description:
4-Chloro-N-sulfinylbenzenamine, identified by its CAS number 13165-68-9, is an organic compound characterized by the presence of a chloro group and a sulfinyl functional group attached to a benzene ring. This compound features a sulfinamide functional group, which is known for its potential applications in medicinal chemistry and as a building block in organic synthesis. The chloro substituent enhances its reactivity, making it a useful intermediate in various chemical reactions, including nucleophilic substitutions. The presence of the sulfinyl group can impart unique properties, such as increased polarity and potential for hydrogen bonding, which may influence its solubility and interaction with biological systems. Additionally, the compound's structure suggests it may exhibit specific biological activities, although detailed studies would be necessary to fully elucidate its pharmacological profile. Overall, 4-Chloro-N-sulfinylbenzenamine represents a versatile compound with potential applications in both research and industry.
Formula:C6H4ClNOS
InChI:InChI=1S/C6H4ClNOS/c7-5-1-3-6(4-2-5)8-10-9/h1-4H
InChI key:InChIKey=GTKDDSPQJMLGOM-UHFFFAOYSA-N
SMILES:N(=S=O)C1=CC=C(Cl)C=C1
Synonyms:- (p-Chlorophenyl)sulfinylamine
- 1-Chloro-4-(sulfinylamino)benzene
- 4-Chloro-N-sulfinylbenzenamine
- 4-Chlorosulfinylaniline
- Aniline, p-chloro-N-sulfinyl-
- N-Sulfinyl-p-chloroaniline
- Thionyl-p-chloroaniline
- benzenamine, 4-chloro-N-sulfinyl-
- p-Chloro-N-sulfinylaniline
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