4741-63-3

Usage

Uses

Used in Pharmaceutical Industry:
6-METHOXY-3 H-ISOBENZOFURAN-1-ONE is used as a pharmaceutical candidate for its potential antioxidant properties, which can help in the development of treatments for various diseases associated with oxidative stress.
Used in Antifungal Applications:
6-METHOXY-3 H-ISOBENZOFURAN-1-ONE is used as an antifungal agent, leveraging its ability to combat fungal infections, which can be crucial in the development of new antifungal drugs.
Used in Organic Synthesis:
6-METHOXY-3 H-ISOBENZOFURAN-1-ONE is used as a building block in the synthesis of various organic compounds, contributing to the creation of new chemical entities with potential applications in different industries.
Used in Industrial Applications:
6-METHOXY-3 H-ISOBENZOFURAN-1-ONE is used as a chemical intermediate in the industrial production of various products, taking advantage of its unique structure to create new materials and compounds.

InChI:InChI=1/C9H8O3/c1-11-7-3-2-6-5-12-9(10)8(6)4-7/h2-4H,5H2,1H3

Upstream product

• 50-00-0 formaldehyd 
• 586-38-9 3-Methoxybenzoic acid 
• 36132-95-3 (2-hydroxymethyl-5-methoxy-phenyl)-methanol 
• 125218-92-0 3,4-dimethoxybenzylidenemethylamine methiodide 
• 125218-88-4 potassium 5-methoxy-3-oxo-1,3-dihydroisobenzofuran-1-carboxylate 
• 65399-19-1 6-methoxy-1-oxo-1,3-dihydroisobenzofuran-3-carboxylic acid 
• 74-95-3 1,1-dibromomethane 

Downstream Products

• 21483-32-9 6-methoxy-7-chloromethylphthalide 
• 76254-25-6 2-cyanomethyl-5-methoxy-benzoic acid 
• 1885-13-8 4-methoxyphthalic acid 
• 4785-56-2 2-formyl-5-methoxy-benzoic acid 
• 28281-76-7 5-methoxyisobenzofuran-1,3-dione 
• 936632-34-7 [2-(hydroxymethyl)-5-methoxyphenyl](2-{[(2-methoxyethoxy)methoxy]methyl}phenyl)methanone 
• 871502-92-0 2-bis(5-methyl-2-furyl)methyl-5-methoxybenzoic acid 
• 52962-25-1 2-(carboxymethyl)-5-methoxybenzoic acid 
• 255376-41-1 5-methoxy-2-methoxycarbonylmethyl-benzoic acid methyl ester 
• 1221486-42-5 2-(3-acetamidophenethyl)-5-methoxybenzoic acid 
• 77620-05-4 methyl 5-methoxyl-2-formylbenzoate 
• 1383781-45-0 (2-(benzyloxymethyl)-5-methoxyphenyl)methanol 
• 1383781-47-2 2-(benzyloxymethyl)-5-methoxybenzaldehyde 
• 1383781-48-3 1-(2-(benzyloxymethyl)-5-methoxyphenyl)heptan-1-ol 

Relevant academic research and scientific papers

Synthesis, characterization and phytotoxic activity of hydroxylated isobenzofuran-1(3H)-ones

Two hydroxylated isobenzofuranones 3 and 4 were synthesized from benzoic acids. The compounds were fully characterized by IR, NMR (1H and 13C), HRMS, and X-ray crystallography. Compounds 3 and 4 crystallized in the space group Pc and

7-Methoxy-3-nitro-2-naphthalenemethanol - A new phototrigger for caging applications

Synthesis, photochemistry and photorelease properties of 7-methoxy-3-nitro-2-naphthalenemethanol (MNNM) are described. Photoirradiation (≥370 nm) of MNNM covalently linked to hippuric acid causes efficient release (～90%) of hippuric acid.

A FACILE SYNTHESIS OF PHTHALIDEISOQUINOLINES BY DECARBOXYLATION OF PHTHALIDECARBOXYLATES IN THE PRESENCE OF IMINE METHIODIDES

Decarboxylation of potassium phthalide-3-carboxylates in the presence of acyclic imine methiodides in DMSO leads mainly to 2-acylbenzamides, but with 3,4-dihydroisoquinolinium methiodides, a one step synthesis of phthalideisoquinolines is achieved in mode

The Oxidation of a Series of Phthalyl Alcohols

A series of phthalyl alcohols containing methoxy and methyl substituents were prepared by lithium aluminum hydride reduction of phthalides.Oxidation of the phthalyl alcohols with activated manganese dioxide or with barium manganate gave phthalaldehydes or