3943-73-5

Basic information

• Product Name: 2,3-DIHYDROXY-BENZOIC ACID ETHYL ESTER
• Synonyms: RARECHEM AL BI 0035;2,3-DIHYDROXY-BENZOIC ACID ETHYL ESTER;ethyl2,3-dihydroxybenzoate;3-(Ethoxycarbonyl)benzene-1,2-diol, 3-(Ethoxycarbonyl)catechol
• CAS NO: 3943-73-5
• Molecular Formula: C₉H₁₀O₄
• Molecular Weight: 182.17
• Product Categories: Esters;Phenyls & Phenyl-Het
• Mol File: 3943-73-5.mol
• Article Data: 9

Chemical Properties

• Melting Point: 65-67°C
• Boiling Point: 307.2°C at 760 mmHg
• Flash Point: 123°C
• Appearance: /
• Density: 1.294g/cm³
• Vapor Pressure: 0.000406mmHg at 25°C
• Refractive Index: 1.573
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 2,3-DIHYDROXY-BENZOIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIHYDROXY-BENZOIC ACID ETHYL ESTER(3943-73-5)
• EPA Substance Registry System: 2,3-DIHYDROXY-BENZOIC ACID ETHYL ESTER(3943-73-5)

Safety Data

• Hazard Codes: Xi:Irritant
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 3943-73-5(Hazardous Substances Data)

Usage

General Description

2,3-Dihydroxy-benzoic acid ethyl ester is a chemical compound with the molecular formula C9H10O4. It is an ethyl ester derivative of 2,3-dihydroxybenzoic acid, which is a naturally occurring phenolic compound found in various plants and fruits. This chemical is commonly used in the pharmaceutical and food industries as a flavoring and fragrance agent. It is also known for its antioxidant properties and has potential applications in the development of drugs and cosmetic products. Additionally, 2,3-dihydroxy-benzoic acid ethyl ester has been studied for its potential therapeutic effects, such as anti-inflammatory and antimicrobial activities.

InChI:InChI=1/C9H10O4/c1-2-13-9(12)6-4-3-5-7(10)8(6)11/h3-5,10-11H,2H2,1H3

Upstream product

• 64-17-5 ethanol 
• 303-38-8 2,3-Dihydroxybenzoic acid 
• 70656-95-0 chlorure de 2,3-dioxosulfinylbenzoyle 
• 102-52-3 malonaldehydebis(dimethylacetal) 
• 120-80-9 benzene-1,2-diol 
• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 
• 66168-85-2 2,3-hydroxybenzoyl chloride 

Downstream Products

• 261767-10-6 ethyl 1,4-benzodioxane-5-carboxylate 
• 303-38-8 2,3-Dihydroxybenzoic acid 

Relevant articles and documents

Efficient synthesis of salicylates by catalytic [3 + 3] cyclizations of 1,3-bis(silyl enol ethers) with 1,1,3,3-tetramethoxypropane

(Chemical Equation Presented) Salicylic acid derivatives were prepared by Me3SiOTf-catalyzed [3 + 3] cyclization of 1,3-bis(silyl enol ethers) with 1,1,3,3-tetramethoxypropane.

Conversion of Simple Cyclohexanones into Catechols

A novel I2-catalyzed direct conversion of cyclohexanones to substituted catechols under mild and simple conditions has been described. This novel transformation is remarkable with the multiple oxygenation and dehydrogenative aromatization processes enabled just by using DMSO as the solvent, oxidant, and oxygen source. This metal-free and simple system demonstrates a versatile protocol for the synthesis of highly valuable substituted catechols and therefore streamlines the synthesis and modification of biologically important molecules for drug discovery.

Structure-activity relationships of neuritogenic gentiside derivatives

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