118-36-5

Usage

Uses

Used in Pharmaceutical Industry:
2-Hydroxydibenzofuran-3-carboxylic acid is used as a pharmaceutical candidate for [application reason], leveraging its unique structure and potential reactivity to develop new drugs and therapies.
Used in Chemical Research:
2-Hydroxydibenzofuran-3-carboxylic acid is used as a research compound for [application reason], exploring its properties, reactivity, and potential applications in various chemical processes and reactions.
Used in Material Science:
2-Hydroxydibenzofuran-3-carboxylic acid is used as a component in the development of new materials for [application reason], such as polymers, coatings, or composites, due to its unique chemical structure and properties.
Note: The specific application reasons for the pharmaceutical, chemical research, and material science industries are not provided in the given materials. They should be filled in based on the actual applications and research findings of 2-hydroxydibenzofuran-3-carboxylic acid.

InChI:InChI=1/C13H8O4/c14-10-5-8-7-3-1-2-4-11(7)17-12(8)6-9(10)13(15)16/h1-6,14H,(H,15,16)

Upstream product

• 86-77-1 2-hydroxydibenzofuran 
• 15719-64-9 methylammonium carbonate 
• 38071-25-9 2-methoxydibenzofuran-3-carboxylic acid 
• 100873-38-9 2-methoxy-dibenzofuran-3-carbonitrile 
• 5834-17-3 3-amino-2-methoxydibenzofuran 

Downstream Products

• 132-62-7 NSC₅₀₅₆₀ 
• 2672-82-4 2-hydroxy-dibenzofuran-3-carboxylic acid-(2,4-dimethoxy-anilide) 
• 3691-93-8 2-hydroxy-dibenzofuran-3-carboxylic acid o-phenetidide 
• 117338-58-6 2-hydroxy-dibenzofuran-3-carboxylic acid anilide 
• 111499-72-0 2-hydroxy-dibenzofuran-3-carboxylic acid o-anisidide 
• 4444-48-8 2-hydroxy-dibenzofuran-3-carboxylic acid-[1]naphthylamide 

Relevant academic research and scientific papers

Syntheses and photophysical properties of fluorescent dibenzofurans, a dibenzothiophene, and carbazoles substituted with bensoxazole and hydroxyl groups to produce excited state intramolecular proton-transfer

Dibenzofurans, a dibenzothiophene, and carbazoles, each substituted with a 2-benzoxazolyl group as well as an ortho-hydroxyl group, were synthesized to produce fluors with fluorescence due to excited-state intramolecular proton-transfer. The orientations for Friedel-Crafts acylation of 3-methoxydibenzothiophene and of the analogous carbazole were determined. The fluors displayed absorption peaks in the 330-385 nm region with molar extinction coefficients up to 57,000. Fluorescence quantum efficiencies of 0.17-0.44 were obtained at wavelengths that had peak values from 540-600 nm. The fluors are of potential use as wavelength shifters in scintillating polystyrene fibers.

Pigment composition

A pigment composition contains a pigment and a dispersant. The dispersant is a phosphoric ester compound represented by the following general formula: wherein at least one of the three Rs is a residuum of a polyester chain containing as principal bonds thereof ester bonds of a polycarboxylic acid and a polyalcohol.

Pigment composition

A pigment composition contains a pigment and a dispersant. The dispersant is a polyester compound which contains, per molecule, a residuum of at least two benzene rings coupled together, an aromatic ring having at least 8 carbon atoms or a heterocyclic ring having at least 8 carbon atoms, and at least one ester bond as a principal bond.