108928-00-3

Basic information

• Product Name: ETHYL 2,4-DIFLUOROBENZOATE
• Synonyms: ETHYL 2,4-DIFLUOROBENZOATE;RARECHEM AL BI 0213;2,4-difluorobenzoic acid ethyl ester;Ethyl 2,4-difluorobenzoate 97%;Ethyl2,4-difluorobenzoate97%
• CAS NO: 108928-00-3
• Molecular Formula: C₉H₈F₂O₂
• Molecular Weight: 186.16
• Product Categories: Aromatic Esters;Benzoic acid;Acids & Esters;Fluorine Compounds
• Mol File: 108928-00-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 65 °C
• Boiling Point: 65 °C
• Flash Point: 65-67°C/15mm
• Appearance: White to light yellow crystal powder
• Density: 1.222
• Refractive Index: 1.4730-1.4770
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: ETHYL 2,4-DIFLUOROBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2,4-DIFLUOROBENZOATE(108928-00-3)
• EPA Substance Registry System: ETHYL 2,4-DIFLUOROBENZOATE(108928-00-3)

Safety Data

• Hazard Codes: Xi,F
• Statements: 36/37/38-37/38-36
• Safety Statements: 26-37-37/39-58-3/9/49-36-15
• HazardClass: IRRITANT, FLAMMABLE
• Hazardous Substances Data: 108928-00-3(Hazardous Substances Data)

Usage

Chemical Properties

White to light yellow crystal powder

Upstream product

• 64-17-5 ethanol 
• 1583-58-0 2,4-difluoro-benzoic acid 

Downstream Products

• 118737-62-5 2,4-difluorobenzoic acid hydrazide 
• 1354961-03-7 4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluorobenzoic acid 
• 1354955-65-9 4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide 

Relevant articles and documents

Tirfluoromethylpyridine oxadiazoles (ether)derivative and application thereof

The invention discloses an application of a tirfluoromethylpyridine oxadiazole (ether)derivative in a pesticide. A structure is shown as a general formula I, a compound shown in the general formula Ihas good insecticidal activity, and can be used for controlling insects such as diamondback moth and armyworm. The compound has excellent control effect for insects such as diamondback moth and armyworm, and also has control effect for the insects having resistance to the traditional pesticides, in addition, introduction of fluorine-containing groups such as tirfluoromethylpyridine and oxadiazoleas well as heterocyclic ring can enhance a rate for forming hydrogen bond effect between a compound and a target, and the activity of the compound is increased.

Bicyclic pyrazole compounds as antibacterial agents

Antibacterial compounds, compositions containing them, and methods of use for the inhibition of bacterial activity and the treatment, prevention or inhibition of bacterial infection.

Synthesis of dibenzoylmethane derivatives and inhibition of mutagenicity in Salmonella typhimurium

Twenty dibenzoylmethanes with methyl, methoxy, bromo, chloro, or fluoro substitution on either one or both benzene rings were synthesized and assayed for inhibition of the mutagenicity of 2-nitrofluorene in S. typhimurium TA98. 2,2-Dimethoxy, 3,3-dimethoxy and 3,3,4,4-tetramethoxydibenzoylmethane was as active as dibenzoylmethane. None of the halogen-substituted dibenzoylmethanes were active. These results demonstrate that dibenzoylmethanes can inhibit the mutagenicity of 2-nitrofluorene, and that modifications made on the benzene rings of dibenzoylmethane cannot enhance the antimutagenicity of this parent compound.