CAS 496-12-8
:Isoindoline
Description:
Isoindoline is a bicyclic organic compound characterized by a fused structure of a benzene ring and a five-membered nitrogen-containing ring. Its molecular formula is C8H7N, indicating the presence of eight carbon atoms, seven hydrogen atoms, and one nitrogen atom. Isoindoline is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It exhibits a distinctive aromatic character due to the presence of the benzene ring, which contributes to its stability and reactivity. Isoindoline can participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic addition, making it a valuable intermediate in organic synthesis. Additionally, it has been studied for its potential applications in pharmaceuticals and materials science, particularly in the development of dyes and agrochemicals. Its unique structure allows for diverse functionalization, which can lead to the creation of novel compounds with specific properties. As with many nitrogen-containing heterocycles, isoindoline's behavior in chemical reactions can be influenced by the presence of substituents on the aromatic ring.
Formula:C8H9N
InChI:InChI=1S/C8H9N/c1-2-4-8-6-9-5-7(8)3-1/h1-4,9H,5-6H2
InChI key:InChIKey=GWVMLCQWXVFZCN-UHFFFAOYSA-N
SMILES:C1=2C(CNC1)=CC=CC2
Synonyms:- 1,3-Dihydro-2H-isoindole
- 1,3-Dihydroisoindole
- 1H-Isoindole, 2,3-dihydro-
- 2,3-dihydro-1H-isoindole
- 2-Azaindan
- Isoindoline
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Found 5 products.
Isoindoline
CAS:Formula:C8H9NPurity:>98.0%(T)Color and Shape:White or Colorless to Light yellow powder to lump to clear liquidMolecular weight:119.17Isoindoline
CAS:<p>Isoindoline is a compound that is used to treat bowel diseases. It is an inhibitor of jak1 and has been shown to be effective in the treatment of inflammatory bowel disease. The reaction mechanism of this drug is not fully understood, but it has been hypothesized that its activity may be due to inhibition of dpp-iv, which blocks the activation of T cells. Isoindoline was found to have low toxicity in h9c2 cells and redox potentials are expected to be low. This drug has also been shown to inhibit the synthesis of fatty acids by inhibiting the action of acyl-coenzyme A: diacylglycerol acyltransferase 2 (ACADS).</p>Formula:C8H9NPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:119.16 g/mol




