28394-58-3

Basic information

• Product Name: Ethyl 3,4-Dichloro Benzoate
• Synonyms: Ethyl 3,4-Dichloro Benzoate
• CAS NO: 28394-58-3
• Molecular Formula: C₉H₈Cl₂O₂
• Molecular Weight: 219.06462
• Mol File: 28394-58-3.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethyl 3,4-Dichloro Benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 3,4-Dichloro Benzoate(28394-58-3)
• EPA Substance Registry System: Ethyl 3,4-Dichloro Benzoate(28394-58-3)

Safety Data

• Hazardous Substances Data: 28394-58-3(Hazardous Substances Data)

Usage

General Description

Ethyl 3,4-Dichloro Benzoate is a chemical compound with the molecular formula C9H7Cl2O2. It is a white crystalline solid commonly used in the production of pharmaceuticals, perfumes, and other organic compounds. The compound is known for its strong and distinctive odor and is often used as a flavoring agent in the food industry. It has also been studied for its potential medicinal properties, with research suggesting it may have anti-inflammatory and antimicrobial effects. Ethyl 3,4-Dichloro Benzoate is considered to be a potentially hazardous chemical and should be handled and stored with caution.

Upstream product

• 64-17-5 ethanol 
• 51-44-5 3,4-dichlorbenzoic acid 
• 32768-54-0 2,3-dichlorotoluene 
• 141-52-6 sodium ethanolate 
• 3024-72-4 3,4-dichlorobenzoyl chloride 
• 75-03-6 ethyl iodide 
• 2642-63-9 3',4'-dichloroacetophenone 
• 6287-38-3 3,4-dichlorobenzaldehyde 

Downstream Products

• 28036-91-1 3,4-dichlorobenzohydrazide 
• 137521-81-4 3-chloro-4-fluoro-benzoic acid ethyl ester 
• 34848-45-8 1,3-di-(3,4-dichlorophenyl)-1,3-propanedione 
• 56882-49-6 5-(3,4-dichlorophenyl)-2,3,5,6-tetrahydroimidazo[2,1-a]isoquinolin-5-ol 
• 2905-68-2 methyl 3,4-dichlorobenzoate 
• 72116-06-4 5-(3,4-dichlorophenyl)-1,3,4-oxadiazole-2(3H)-one 

Relevant articles and documents

Synthesis, spectral characterization, and biological studies of 3,5-disubstituted-1,3,4-oxadiazole-2(3H)-thione derivatives

The reaction of 3,4-dichlorophenyl-1,3,4-oxadiazole-2(3H)-thione with piperidine derivatives via Mannich reaction was used to generate eleven novel compounds in moderate to good yields. Synthesized molecules were characterized according to their structure

Some Novel Mannich Bases of 5-(3,4-Dichlorophenyl)-1,3,4-oxadiazole-2(3H)-one and Their Anti-Inflammatory Activity

Non-steroidal anti-inflammatory drugs (NSAIDs), which are widely used for the treatment of rheumatic arthritis, pain, and many different types of inflammatory disorders, cause serious gastrointestinal (GI) side effects. The free carboxylic acid group exis

Synthesis, characterization and anti-inflammatory activity of new 5- (3,4-dichlorophenyl)-2-(aroylmethyl) thio-1,3,4-oxadiaxoles

Several 5-(3,4-dichlorophenyl)-2-(aroylmethyl)thio-1,3,4-oxadiazoles were synthesized and characterized by elemental analyses, IR and nuclear magnetic resonance spectra. All compounds were evaluated for anti-inflammatory activity by determining their abil