6843-89-6

Usage

Uses

Used in Dye and Pigment Manufacturing:
Ethyl-1,3-dihydroxy-2-naphthoate is used as a dye intermediate for the production of various dyes and pigments. Its chemical properties allow it to be a crucial component in the synthesis of colorants that are used in different industries.
Used in Textile Industry:
In the textile industry, Ethyl-1,3-dihydroxy-2-naphthoate is used as a colorant to impart specific shades and hues to fabrics. Its role in dye manufacturing makes it instrumental in creating vibrant and long-lasting colors for textiles.
Used in Cosmetics Industry:
Ethyl-1,3-dihydroxy-2-naphthoate is also used as a colorant in the cosmetics industry, where it helps in creating a wide range of colors for various cosmetic products while ensuring safety and low toxicity.
Used in Printing and Ink Industry:
In the printing and ink industry, Ethyl-1,3-dihydroxy-2-naphthoate is utilized as a component in ink formulations, contributing to the color intensity and quality of the printed materials.
Used in Plastics and Polymers Industry:
Ethyl-1,3-dihydroxy-2-naphthoate serves as a colorant in the plastics and polymers industry, where it is used to add color to various plastic products, ensuring both aesthetic appeal and product differentiation.

InChI:InChI=1/C13H12O4/c1-2-17-13(16)11-10(14)7-8-5-3-4-6-9(8)12(11)15/h3-7,14-15H,2H2,1H3

Upstream product

• 20320-59-6 diethyl 2-(2-phenylacetyl)malonate 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 105-50-0 diethyl 1,3-acetonedicarboxylate 

Downstream Products

• 3147-58-8 1,3-dihydroxy-[2]naphthoic acid 
• 10075-61-3 1,3-dimethoxynaphthalene 
• 132-86-5 1,3-dihydroxynaphthalene 

Relevant academic research and scientific papers

Transition-Metal-Free Benzannulation of Tricarbonyl Derivatives with Arynes: Access to 1,3-Dinaphthol Precursors for the Synthesis of Rhodamine Dye Analogues

Herein, we report a transition-metal-free annulation reaction of benzynes and 1,3-oxopentanedioate for the synthesis of highly functionalized naphthalene derivatives for the first time. Additionally, the representative naphthalene derivatives have been successfully transformed into the new series of rhodamine dye analogues.

The Interrupted Pummerer Reaction in a Sulfoxide-Catalyzed Oxidative Coupling of 2-Naphthols

A benzothiophene S-oxide catalyst, generated in situ by sulfur oxidation with H2O2, mediates the oxidative coupling of 2-naphthols. Key to the catalytic process is the capture and inversion of reactivity of a 2-naphthol partner, using an interrupted Pummerer reaction of an unusual benzothiophene S-oxide, followed by subsequent coupling with a second partner. The new catalytic manifold has been showcased in the synthesis of the bioactive natural products, (±)-nigerone and (±)-isonigerone. Although Pummerer reactions are used widely, their application in catalysis is rare, and our approach represents a new catalytic manifold for metal-free C?C bond formation.

Comprehensive study on excited state intramolecular proton transfer in 2-(benzo[d]thiazol-2-yl)-3-methoxynaphthalen-1-ol and 2-(benzo[d]thiazol-2-yl)naphthalene-1,3-diol: Effect of solvent, aggregation, viscosity and TDDFT study

Three compounds DMT, MMT and DHT having dimehtoxy, mono-hydroxy and di-hydroxy groups respectively were prepared. Environmental interactions dependent photophysical properties especially excited state intramolecular proton transfer (ESIPT), solvatochromism, aggregation induced emission enhancement (AIEE) and viscosity dependent emission characteristics were studied. The effect of solvent polarity on ESIPT dynamics were studied using UV–vis and emission spectroscopy along with aggregation induced enhanced emission and viscosity effect. MMT and DHT showed unexpected and contrasting behavior in the solvents which are in good agreement with the density functional theory and time dependent density functional theory findings. Aggregation and viscosity study showed that cis-keto emission increased drastically in the aggregate state and highly viscous state due to restricted intramolecular rotation increasing the population of required cis enol rotamer (E). The study directs the potential applications of such molecules for advanced optoelectronics and viscosity based investigations.

Novel Inhibitors of Hepatitis C Virus Replication

The embodiments provide compounds of the general Formula I, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.