CAS 267-48-1
:5H-1,3-Dioxolo[4,5-f]indole
Description:
5H-1,3-Dioxolo[4,5-f]indole, with the CAS number 267-48-1, is a heterocyclic organic compound characterized by its fused dioxole and indole structures. This compound typically exhibits a bicyclic framework, which contributes to its unique chemical properties. It is known for its potential applications in organic synthesis and medicinal chemistry, particularly due to its ability to participate in various chemical reactions, including electrophilic substitutions and cycloadditions. The presence of the dioxole moiety can enhance its reactivity and influence its electronic properties, making it a subject of interest in the development of new materials and pharmaceuticals. Additionally, compounds of this type may exhibit interesting biological activities, although specific biological data may vary. Its stability, solubility, and reactivity can be influenced by substituents on the indole or dioxole rings, making it a versatile building block in synthetic organic chemistry. Overall, 5H-1,3-Dioxolo[4,5-f]indole represents a fascinating area of study within the field of heterocyclic chemistry.
Formula:C9H7NO2
InChI:InChI=1/C9H7NO2/c1-2-10-7-4-9-8(3-6(1)7)11-5-12-9/h1-4,10H,5H2
InChI key:InChIKey=HXCHORPNRVSDCD-UHFFFAOYSA-N
SMILES:C=12C(=CC3=C(C1)OCO3)NC=C2
Synonyms:- 1H-Indole, 5,6-[methylenebis(oxy)]-
- 2H,5H-[1,3]Dioxolo[4,5-f]indole
- 5,6-(Methylenedioxy)indole
- 5,6-Methylenedioxy-1H-indole
- 5,6-Methylenedioxyindole
- 5H-1,3-Dioxolo(4,5-f)indole
- 8aH-[1,3]dioxolo[4,5-f]indole
- Brn 0132678
- Nsc 92516
- 4-27-00-06314 (Beilstein Handbook Reference)
- 5-6-methylenedioxyindole tan crystals
- See more synonyms
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Found 4 products.
5H-[1,3]Dioxolo[4,5-f]indole
CAS:Formula:C9H7NO2Purity:97%Color and Shape:SolidMolecular weight:161.15745H-[1,3]Dioxolo[4,5-f]indole
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:161.160003662109385,6-Methylenedioxyindole
CAS:<p>5,6-Methylenedioxyindole (MDI) is a compound that is often used in the synthesis of other bioactive molecules. It has been shown to bind to the pyridinium moiety of receptor sites and form a stable complex, which can then be displaced by an agonist or antagonist. The binding experiments were performed using radioactive MDI and zoxazolamine as the ligand. Radiolabelled MDI was synthesized from 5-methyl-2-pyridinone with the use of a linker, methylenetriphenylphosphorane (MTPP). The molecular electrostatic potentials of the two compounds were calculated in order to investigate the possible binding interactions between them. Ellipticines are also synthesised using MDI as a precursor molecule, which is alkylated with dimethyl sulfate and then reacted with phenylhydrazine. This reaction produces a mixture containing both ellipticines and</p>Formula:C9H7NO2Purity:Min. 95%Molecular weight:161.16 g/mol



