CAS 4720-68-7
:1,3-Benzodioxole-5-carboxaldehyde, 6-hydroxy-
Description:
1,3-Benzodioxole-5-carboxaldehyde, 6-hydroxy- is an organic compound characterized by its unique bicyclic structure, which consists of a benzodioxole moiety and an aldehyde functional group. This compound features a hydroxyl group at the 6-position, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid or solid, depending on the specific conditions and purity. The presence of both the aldehyde and hydroxyl groups makes it a versatile intermediate in the synthesis of various pharmaceuticals and agrochemicals. Additionally, its structure allows for potential hydrogen bonding and interactions with other molecules, which can influence its solubility and reactivity in different solvents. The compound is of interest in research for its potential biological activities, including antimicrobial and antioxidant properties. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled.
Formula:C8H6O4
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Found 4 products.
1,3-Benzodioxole-5-carboxaldehyde, 6-hydroxy-
CAS:Formula:C8H6O4Purity:98%Color and Shape:SolidMolecular weight:166.13086-Hydroxy-2H-1,3-benzodioxole-5-carbaldehyde
CAS:6-Hydroxy-2H-1,3-benzodioxole-5-carbaldehydePurity:98%Molecular weight:166.13084g/mol6-hydroxybenzo[d][1,3]dioxole-5-carbaldehyde
CAS:Formula:C8H6O4Purity:98%Color and Shape:SolidMolecular weight:166.1326-Hydroxy-1,3-dioxaindane-5-carbaldehyde
CAS:6-Hydroxy-1,3-dioxaindane-5-carbaldehyde is a crystalline compound that belongs to the group of benzo dioxoles. The compound has a planar structure with a single bond between carbons 1 and 3 and double bonds between carbons 2 and 4 and 5. The molecule has an asymmetric center in the benzodioxole ring system. This molecule has an electrostatic charge on the carbonyl groups due to the electronegativity of oxygen.Formula:C8H6O4Purity:Min. 95%Molecular weight:166.13 g/mol



