98191-30-1

Basic information

• Product Name: 3,5-Dichloro-4-fluorobenzoic acid
• Synonyms: 3,5-Dichloro-4-fluorobenzoicacid
• CAS NO: 98191-30-1
• Molecular Formula: C₇H₃Cl₂FO₂
• Molecular Weight: 209.00
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;Fluorine series
• Mol File: 98191-30-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 317.7 °C at 760 mmHg
• Flash Point: 146 °C
• Appearance: /
• Density: 1.606
• Vapor Pressure: 0.000158mmHg at 25°C
• Refractive Index: 1.574
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3,5-Dichloro-4-fluorobenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Dichloro-4-fluorobenzoic acid(98191-30-1)
• EPA Substance Registry System: 3,5-Dichloro-4-fluorobenzoic acid(98191-30-1)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 98191-30-1(Hazardous Substances Data)

Usage

General Description

3,5-Dichloro-4-fluorobenzoic acid is a chemical compound with the molecular formula C7H3Cl2FO2. It is a derivative of benzoic acid and contains two chlorine atoms and one fluorine atom attached to the benzene ring. 3,5-Dichloro-4-fluorobenzoic acid is used in the synthesis of pharmaceuticals and agrochemicals. It is also utilized as an intermediate in the production of dyes and pigments. Additionally, 3,5-Dichloro-4-fluorobenzoic acid has been studied for its potential use in corrosion inhibition and as a building block for the synthesis of new materials with specific physicochemical properties.

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

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

Relevant articles and documents

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.

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.