Sulfamoyl chloride, specifically the compound with the name "[(2,3-dihydro-1H-indol-1-yl)carbonyl]-", is an organic compound characterized by the presence of a sulfonamide functional group attached to a carbonyl moiety linked to a dihydroindole structure. This compound typically exhibits properties associated with both sulfonamides and amides, including potential reactivity towards nucleophiles due to the electrophilic carbonyl carbon. It is likely to be a solid at room temperature and may be sensitive to moisture, which can lead to hydrolysis of the sulfonyl chloride group. The presence of the indole moiety suggests potential biological activity, as indole derivatives are known for their roles in pharmaceuticals and agrochemicals. The compound may be utilized in synthetic organic chemistry for the preparation of more complex molecules, particularly in medicinal chemistry. Safety precautions should be taken when handling this compound, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or amines.

Sulfamoyl chloride, [(2,3-dihydro-1H-indol-1-yl)carbonyl]-

89731-80-6: Sulfamoyl chloride, specifically the compound with the name "[(2,3-dihydro-1H-indol-1-yl)carbonyl]-", is an organic compound characterized by the presence of a sulfonamide functional group attached to a carbonyl moiety linked to a dihydroindole structure. This compound typically exhibits properties associated with both sulfonamides and amides, including potential reactivity towards nucleophiles due to the electrophilic carbonyl carbon. It is likely to be a solid at room temperature and may be sensitive to moisture, which can lead to hydrolysis of the sulfonyl chloride group. The presence of the indole moiety suggests potential biological activity, as indole derivatives are known for their roles in pharmaceuticals and agrochemicals. The compound may be utilized in synthetic organic chemistry for the preparation of more complex molecules, particularly in medicinal chemistry. Safety precautions should be taken when handling this compound, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or amines.

CAS 89731-80-6

Sulfamoyl chloride, [(2,3-dihydro-1H-indol-1-yl)carbonyl]-

Sulfamoyl chloride, [(2,3-dihydro-1H-indol-1-yl)carbonyl]-

Ref: IN-DA0041T5