3,4-Dihydro-2H-1,5-benzodioxepin-7-yl(phenyl)methanol, with the CAS number 5786-82-3, is a chemical compound characterized by its unique structural features, which include a benzodioxepin core and a phenylmethanol moiety. This compound typically exhibits a molecular structure that combines both aromatic and aliphatic characteristics, contributing to its potential reactivity and interactions. It is often studied for its pharmacological properties, as compounds with similar structures may exhibit biological activity, including anti-inflammatory or analgesic effects. The presence of hydroxyl (-OH) groups in its structure can enhance solubility in polar solvents and may influence its binding affinity to biological targets. Additionally, the compound's stereochemistry can play a crucial role in its biological activity and interactions. As with many organic compounds, its stability, solubility, and reactivity can vary based on environmental conditions such as pH and temperature. Overall, 3,4-dihydro-2H-1,5-benzodioxepin-7-yl(phenyl)methanol represents a class of compounds of interest in medicinal chemistry and organic synthesis.

3,4-dihydro-2H-1,5-benzodioxepin-7-yl(phenyl)methanol

5786-82-3: 3,4-Dihydro-2H-1,5-benzodioxepin-7-yl(phenyl)methanol, with the CAS number 5786-82-3, is a chemical compound characterized by its unique structural features, which include a benzodioxepin core and a phenylmethanol moiety. This compound typically exhibits a molecular structure that combines both aromatic and aliphatic characteristics, contributing to its potential reactivity and interactions. It is often studied for its pharmacological properties, as compounds with similar structures may exhibit biological activity, including anti-inflammatory or analgesic effects. The presence of hydroxyl (-OH) groups in its structure can enhance solubility in polar solvents and may influence its binding affinity to biological targets. Additionally, the compound's stereochemistry can play a crucial role in its biological activity and interactions. As with many organic compounds, its stability, solubility, and reactivity can vary based on environmental conditions such as pH and temperature. Overall, 3,4-dihydro-2H-1,5-benzodioxepin-7-yl(phenyl)methanol represents a class of compounds of interest in medicinal chemistry and organic synthesis.

Tetrahydrohomofolic acid is a thymidylate synthetase inhibitor, antibacterial, and antimalarial agent.

CAS 5786-82-3

3,4-dihydro-2H-1,5-benzodioxepin-7-yl(phenyl)methanol

Tetrahydrohomofolic acid

Ref: TM-T26261