CAS 166883-20-1
:1-Methyl-2-oxo-5-indolinesulfonyl chloride
Description:
1-Methyl-2-oxo-5-indolinesulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and ability to form sulfonamides. This compound features an indoline structure, which contributes to its unique properties and potential applications in organic synthesis and medicinal chemistry. The presence of the methyl and keto groups enhances its reactivity, making it useful in various chemical reactions, including acylation and sulfonylation. As a sulfonyl chloride, it can act as a versatile electrophile, allowing for the introduction of sulfonyl groups into other molecules. The compound is typically handled with care due to its reactive nature, particularly in the presence of moisture, which can lead to hydrolysis. Its applications may extend to the development of pharmaceuticals or agrochemicals, where the indoline moiety can impart biological activity. Overall, 1-Methyl-2-oxo-5-indolinesulfonyl chloride is a valuable intermediate in synthetic organic chemistry.
Formula:C9H8ClNO3S
InChI:InChI=1/C9H8ClNO3S/c1-11-8-3-2-7(15(10,13)14)4-6(8)5-9(11)12/h2-4H,5H2,1H3
SMILES:CN1c2ccc(cc2CC1=O)S(=O)(=O)Cl
Synonyms:- 1-Methyl-2-oxoindoline-5-sulphonyl chloride
- 1-Methyl-2-oxoindoline-5-sulphonyl chloride 95%
- 1-methyl-2-oxo-2,3-dihydro-1H-indole-5-sulfonyl chloride
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Found 4 products.
1H-Indole-5-sulfonyl chloride, 2,3-dihydro-1-methyl-2-oxo-
CAS:Formula:C9H8ClNO3SPurity:96%Color and Shape:SolidMolecular weight:245.68271-Methyl-2-oxindole-5-sulphonyl chloride
CAS:<p>1-Methyl-2-oxindole-5-sulphonyl chloride</p>Formula:C9H8ClNO3SPurity:95%Color and Shape: beige solidMolecular weight:245.68g/mol1-Methyl-2-oxo-2,3-dihydro-1H-indole-5-sulfonyl chloride
CAS:Formula:C9H8ClNO3SPurity:96%Color and Shape:SolidMolecular weight:245.681-Methyl-2-oxindole-5-sulphonyl chloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H8ClNO3SPurity:Min. 95%Molecular weight:245.68 g/mol



