137640-94-9

Usage

Uses

Used in Organic Synthesis:
6-Chloro-N-(4-fluorophenyl)-2-pyridinecarboxamide is used as a building block for the synthesis of more complex organic molecules. Its unique structural features make it a valuable intermediate in the preparation of various compounds.
Used in Pharmaceutical Research:
6-Chloro-N-(4-fluorophenyl)-2-pyridinecarboxamide is used as a starting material in the development of new drugs. Its potential pharmacological properties, such as its ability to interact with biological targets, make it a promising candidate for further research and development in the pharmaceutical industry.
Used in Agrochemical Development:
6-Chloro-N-(4-fluorophenyl)-2-pyridinecarboxamide is used as a potential component in the development of new agrochemicals. Its structural features may contribute to the creation of novel compounds with improved properties for use in agriculture, such as pesticides or herbicides.
Further research is needed to determine the specific uses and potential benefits of 6-Chloro-N-(4-fluorophenyl)-2-pyridinecarboxamide in various fields, as its applications are currently under exploration.

Upstream product

• 1929-82-4 nitrapyrin 
• 371-40-4 4-fluoroaniline 
• 4684-94-0 6-chloropicolinic acid 
• 80099-98-5 6-chloropicolinoyl chloride 
• 79-24-3 Nitroethane 

Downstream Products

• 157328-20-6 N-(4-fluorophenyl)-2-(1',3'-dimethylpyrazol-5'-yloxy)-6-pyridinecarboxamid 
• 137641-05-5 N-(4-fluorophenyl)-6-(3-trifluoromethylphenoxy)pyridine-2-carboxamide 

Relevant academic research and scientific papers

Method for preparing amide through electrochemical dechlorination of trichloromethyl pyridine derivative

The invention discloses a method for preparing amide by electrochemical dechlorination of a trichloromethylpyridine derivative, the method is characterized by comprising the following steps of: (1) dissolving a polychloropyridine derivative in an amine so

PROCESS FOR THE PREPARATION OF PYRIDYLCARBOXYLIC AMIDES AND ESTERS

The invention relates to a process for the preparation of pyridylcarboxylic amides and esters I, Formula (I) wherein Hal, X and R1 have the meanings given in claim 1, which comprises the following steps: (a) heating a mixture consisting essenti

Herbicidal carboxamide derivatives

The invention provides compounds of the general formula in whichR1 represents a hydrogen or halogen atom or an alkyl or haloalkyl group;the or each group X independently represents a halogen atom or an optionally substituted alkyl or alkoxy group or an alkenyloxy, alkynyloxy, cyano, carboxy, alkoxycarbonyl, (alkylthio)carbonyl, alkylcarbonyl, amido, alkylamido, nitro, alkylthio, haloalkylthio, alkenylthio, alkynylthio, alkylsulphinyl, alkylsulphonyl, alkyloximinoalkyl or alkenyloximinoalkyl group;n is 0 or an integer from 1 to 5; andL is an alkoxy group.

Preparation of hetero arylcarboxamides

The invention relates to a process for the preparation of heteroarylcarboxylic amides and esters of formula I in which one or two of the groups A1, A2, A3, A4, and A5 represent a nitrogen atom and the other groups each independently represent CR3, Hal rep

Process for the preparation of heteroarylcarboxylic amides and esters

The invention relates to a process for the preparation of heteroarylcarboxylic amides and esters of formula I in which A1through A5, R1, Hal and X one or twoof the groups A1, A2, A3, A

Herbicidal picolinamide derivatives

Herbicidal picolinamide derivatives are provided having the formula I STR1 which Z represents an oxygen or sulphur atom, R1 and R2 each independently represents a hydrogen atom or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aryl, aralkyl, alkaryl, hydroxy, alkoxy, alkenyloxy, alkynyloxy, alkylcarbonyl, amino, mono- or di-alkylamino, alkoxycarbonylamino, arylamino, arylalkylamino or dialkylcarbamoyl group, or together represent an alkylene chain which is optionally interrupted by an oxygen or sulphur atom or by a group --NR-- in which R represents a hydrogen atom or an alkyl group, R3 independently represents a halogen atom or an alkyl or haloalkyl group, R4, R5 and R6 each independently represents a hydrogen or halogen atom, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aryl, aralkyl, alkaryl, alkoxy, amino, mono- or di-alkylamino, alkoxycarbonylamino, arylamino, dialkylcarbamoyl, acyl or acylamido group or a cyano group, with the proviso that R5 and R6 do not represent an acyl, acylamido or cyano group, and n represents 0, 1, 2 or 3.

Process for the preparation of acid chloride compounds

A process for preparing a compound of general formula STR1 where Ar represents an optionally substituted aromatic or heteroaromatic group, the process comprising reacting a compound of general formula where each L1 independently represents a leaving group (preferably a chlorine atom), with water in the presence of a Lewis acid and a chlorocarbon solvent which includes at least two chlorine atoms, is disclosed.

Herbicidal picolinamide derivatives

Compounds of the formula: STR1 wherein R1 and R2 each independently represents hydrogen, optionally substituted alkyl, aryl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aralkyl, alkaryl, hydroxy, alkoxy, alkenyloxy, alkynyloxy, al