CAS 3074-25-7

1H-Indole-6-sulfonamide,2,3-dihydro-

Description:

1H-Indole-6-sulfonamide, 2,3-dihydro- is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of a sulfonamide group (-SO2NH2) indicates that it possesses sulfonamide characteristics, which often contribute to its biological activity. This compound typically exhibits properties such as solubility in polar solvents, and it may have moderate to low solubility in non-polar solvents. The indole moiety is known for its role in various biological processes and can be involved in interactions with biological targets, making such compounds of interest in medicinal chemistry. Additionally, the dihydro form suggests that it has undergone hydrogenation, which may influence its reactivity and stability. Overall, 1H-Indole-6-sulfonamide, 2,3-dihydro- is a compound of interest in pharmaceutical research, particularly for its potential therapeutic applications.

Formula: C₈H₁₀N₂O₂S

Synonyms:

• 6-Indolinesulfonamide(7CI,8CI)

2,3-Dihydro-1H-indole-6-sulfonamide

CAS: 3074-25-7

2,3-Dihydro-1H-indole-6-sulfonamide is a carboxylate antibiotic that has been shown to be active against a variety of bacteria including Staphylococcus and Streptococcus. The enzyme activity of the drug is related to the nature of the carboxylates. 2,3-Dihydro-1H-indole-6-sulfonamide has a unique chemical structure that includes both amines and piperidine, which may explain its inhibitory potency. The active site for this drug is in the indoline ring, which contains an oxygen atom with a double bond between carbons 1 and 2.

Formula: C₈H₁₀N₂O₂S

Purity: Min. 95%

Molecular weight: 198.24 g/mol

Ref: 3D-DAA07425