98191-30-1

Usage

Uses

Used in Pharmaceutical Industry:
3,5-Dichloro-4-fluorobenzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to advancements in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-Dichloro-4-fluorobenzoic acid serves as an essential building block for the creation of novel agrochemicals. Its incorporation into these products can enhance their effectiveness in agricultural applications, such as pest control and crop protection.
Used in Dye and Pigment Production:
3,5-Dichloro-4-fluorobenzoic acid is utilized as an intermediate in the production of dyes and pigments. Its presence in these compounds can impart specific color characteristics and improve their performance in various applications, such as textiles, plastics, and inks.
Used in Corrosion Inhibition:
3,5-Dichloro-4-fluorobenzoic acid has been studied for its potential use in corrosion inhibition. Its chemical properties may offer protective effects against corrosion in various materials, making it a valuable component in the development of corrosion-resistant coatings and treatments.
Used in Material Science:
As a building block for the synthesis of new materials, 3,5-Dichloro-4-fluorobenzoic acid contributes to the development of materials with specific physicochemical properties. Its unique structure can be leveraged to create innovative materials with tailored characteristics for use in various industries, such as electronics, aerospace, and automotive.

InChI:InChI=1/C7H3Cl2FO2/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2H,(H,11,12)

Upstream product

• 77227-81-7 1,3-dichloro-2-fluoro-5-(trifluoromethyl)benzene 

Downstream Products

• 115551-95-6 ethyl 3,5-dichloro-4-fluorobenzoate 
• 887577-44-8 3,5-dichloro-4-hydrazinobenzoic acid 
• 755014-50-7 3,5-dichloro-4-fluorobenzoyl chloride 
• 957828-47-6 (3,5-dichloro-4-fluoro-benzoylamino)-acetic acid tert-butyl ester 

Relevant academic research and scientific papers

Bioavailable diacylhydrazine ligands for modulating the expression of exogenous genes via an ecdysone receptor complex

The present invention relates to non-steroidal ligands for use in nuclear receptor-based inducible gene expression system, and a method to modulate exogenous gene expression in which an ecdysone receptor complex comprising: a DNA binding domain; a ligand binding domain; a transactivation domain; and a ligand is contacted with a DNA construct comprising: the exogenous gene and a response element; wherein the exogenous gene is under the control of the response element and binding of the DNA binding domain to the response element in the presence of the ligand results in activation or suppression of the gene.

N-[phenyl (piperidin-2-yl) methyl]benzamide derivatives, preparation thereof, and use thereof in therapy

This invention discloses and claims a compound of general formula (I) in which R1 represents either a hydrogen atom, or an optionally substituted alkyl group, or a cycloalkylalkyl group, or an optionally substituted phenylalkyl group, or an alk

Phenyl pyridones and insectidal use thereof

A compound of formula (I) STR1 wherein R1, R2, R4 and R5 are independently selected from hydrogen, halogen, lower alkyl optionally substituted by halogen, lower alkoxy optionally substituted by halogen and lower alkenyl optionally substituted by halogen; R3 is halogen, amino, mono- or di(lower alkyl)-amino, lower alkyl substituted by halogen, lower alkoxy optionally substituted by halogen and lower alkenyl optionally substituted by halogen provided that R3 is not monochloro or monobromo-methyl; R6 is oxygen or sulphur; R7 and R10 are independently selected from hydrogen, halogen, lower alkyl optionally substituted by halogen, lower alkoxy optionally substituted by halogen, and lower thioalkoxy optionally substituted by halogen; and R8 is hydrogen, halogen, optionally substituted lower alkyl, optionally substituted lower alkoxy, optionally substituted lower thioalkoxy, cyano, nitro, optionally substituted oximino, optionally substituted lower alkenyl, optionally substituted aryloxy, optionally substituted amino or S(O)nR11 wherein n is 0, 1 or 2 and R11 is optionally substituted lower alkyl; R9 is hydrogen, or lower alkyl optionally substituted by halogen, lower alkenyl optionally substituted by halogen or CO2 R12 wherein R12 is lower alkyl optionally substituted by halogen; provided that R1, R2, R3, R4 and R5 are not all hydrogen; and further provided that when R3 is trifluoromethyl and R1 and R5 are halogen, R2 and R4 are not both hydrogen, or R7, R8, R9 and R10 do not comprise from one to four halogen or trihalomethyl substituents.