CAS 61658-41-1

Naphtho[1,2-b]furan-4-carboxylic acid,5-hydroxy-,methyl ester

Description:

Naphtho[1,2-b]furan-4-carboxylic acid, 5-hydroxy-, methyl ester is an organic compound characterized by its complex polycyclic structure, which includes a naphthalene ring fused to a furan moiety. This compound features a carboxylic acid functional group that is esterified with a methanol molecule, resulting in a methyl ester. The presence of a hydroxyl group at the 5-position of the naphtho-furan structure contributes to its potential reactivity and solubility properties. Typically, compounds of this nature exhibit interesting biological activities, making them of interest in pharmaceutical and chemical research. They may also display unique optical properties due to their conjugated system. The compound's molecular structure suggests it could participate in various chemical reactions, including esterification and oxidation. Additionally, its CAS number, 61658-41-1, allows for precise identification in chemical databases, facilitating research and application in various fields, including organic synthesis and medicinal chemistry.

Furomollugin

CAS: 61658-41-1

Formula: C₁₄H₁₀O₄

Purity: 98.0%

Color and Shape: Solid

Molecular weight: 242.2268

Ref: IN-DA00EGUM

Furomollugin

CAS: 61658-41-1

Furomollugin has antiviral activity, it can strongly suppress the secretion of hepatitis B surface antigen (HBsAg), with IC50 = 2.0 micrograms/mL, in human

Formula: C₁₄H₁₀O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 242.23

Ref: TM-TN2417

Furomollugin

CAS: 61658-41-1

Formula: C₁₄H₁₀O₄

Purity: 95%~99%

Color and Shape: Cryst.

Molecular weight: 242.23

Ref: BP-SBP60002

Furomollugin

CAS: 61658-41-1

Furomollugin is a bioactive compound derived from natural sources, specifically isolated from certain plant species known for their medicinal properties. It is classified as a secondary metabolite, indicating its involvement in the plant's defense mechanisms. The mode of action of Furomollugin involves interacting with specific cellular pathways to exert biological effects. This interaction may include modulation of enzymatic activity or interference with signal transduction pathways, which can lead to various therapeutic outcomes.

Formula: C₁₄H₁₀O₄

Purity: Min. 95%

Molecular weight: 242.23 g/mol

Ref: 3D-LCA65841