CAS 222036-66-0
:5-amino-2,3-dihydro-1H-isoindol-1-one
Description:
5-amino-2,3-dihydro-1H-isoindol-1-one, with the CAS number 222036-66-0, is a heterocyclic organic compound characterized by its isoindole structure, which features a fused benzene and pyrrole ring. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents. The presence of an amino group contributes to its potential reactivity, allowing for various chemical modifications. It may participate in hydrogen bonding due to the amino and carbonyl functionalities, influencing its solubility and interaction with biological systems. The compound is of interest in medicinal chemistry, particularly for its potential pharmacological properties, including anti-inflammatory and neuroprotective effects. Its structural features may also allow it to act as a scaffold for the development of novel therapeutic agents. As with many organic compounds, safety and handling precautions should be observed, as its biological effects and toxicity profiles may vary depending on concentration and exposure routes.
Formula:C8H8N2O
InChI:InChI=1/C8H8N2O/c9-6-1-2-7-5(3-6)4-10-8(7)11/h1-3H,4,9H2,(H,10,11)
SMILES:c1cc2c(cc1N)CNC2=O
Synonyms:- 1H-Isoindol-1-one, 5-amino-2,3-dihydro-
- 5-Aminoisoindolin-1-one
- 5-Aminoisoindoline-1-One
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Found 4 products.
5-Aminoisoindolin-1-one
CAS:<p>5-Aminoisoindolin-1-one</p>Formula:C8H8N2OPurity:97%Color and Shape: yellow solidMolecular weight:148.16g/mol5-Amino-2,3-dihydro-1H-isoindol-1-one
CAS:Formula:C8H8N2OPurity:95%Color and Shape:SolidMolecular weight:148.1655-Aminoisoindolin-1-one
CAS:<p>5-Aminoisoindolin-1-one is an antibiotic agent with a broad spectrum of activity. It has been shown to inhibit transcription of the methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant Staphylococcus aureus (MRSA) profiles, as well as transcriptional and translational activities of Streptococcus epidermidis and Streptococcus pyogenes. 5-Aminoisoindolin-1-one inhibits bacterial growth by binding to ribosomes, preventing protein synthesis and cell division. Its antibacterial properties have been shown using in vitro experiments to inhibit the growth of MSSA, MRSA, Streptococcus epidermidis, Streptococcus pyogenes, and Escherichia coli. This drug also integrates into RNA molecules and may be effective against bacteria that are resistant to other antibiotics.</p>Formula:C8H8N2OPurity:Min. 95%Molecular weight:148.16 g/mol



