84282-78-0

Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-4-Fluorophenylhydrazine is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Research:
In the field of chemical research, 3-Chloro-4-Fluorophenylhydrazine serves as a valuable compound for studying the properties and reactions of phenylhydrazines and their derivatives. It can be used to explore the reactivity of the halogen atoms and the influence of the phenyl group on the overall chemical behavior of the molecule.
Used in Material Science:
3-Chloro-4-Fluorophenylhydrazine may be utilized in the development of new materials with specific properties, such as improved stability or reactivity. Its potential applications in material science could include the creation of novel catalysts, sensors, or other advanced materials that benefit from the unique characteristics of 3-CHLORO-4-FLUOROPHENYLHYDRAZINE.

InChI:InChI=1/C6H6ClFN2/c7-5-3-4(10-9)1-2-6(5)8/h1-3,10H,9H2

Upstream product

• 367-21-5 3-chloro-4-fluorophenylamine 

Downstream Products

• 84304-75-6 2-(3-chloro-4-fluorophenyl)hydrazinecarboxylic acid ethyl ester 
• 84304-77-8 N'-(3-Chloro-4-fluoro-phenyl)-hydrazinecarboxylic acid phenyl ester 
• 442520-02-7 1-(3-chloro-4-fluoro-phenylamino)-pyrrole-2,5-dione 
• 175135-53-2 5-amino-1-(3-chloro-4-fluorophenyl)-4-cyanopyrazole 
• 84282-58-6 5-ethoxy-3-(3-chloro-4-fluorophenyl)-1,3,4-oxadiazol-2(3H)-one 
• 1431772-01-8 (E)-methyl3-(2-(3-chloro-4-fluorophenyl)-2H-1,2,3-triazol-4-yl)acrylate N-oxide 
• 1431772-03-0 (E)-butyl3-(2-(3-chloro-4-fluorohenyl)-2H-1,2,3-triazol-4-yl)acrylate N-oxide 
• 1431772-10-9 2-(3-chloro-4-fluorophenyl)-2H-1,2,3-triazole N-oxide 
• 1610689-80-9 N'-(3-chloro-4-fluorophenyl)acetohydrazide 

Relevant academic research and scientific papers

Selective reduction of aryl diazonium fluoroborates

Substituted aryl diazonium fluoroborates have been selectively reduced to the corresponding phenylhydrazines by using borohydride exchange resin (BER).

Preparation of 2-phenylsemicarbazides

2-Phenylsemicarbazides are prepared by a multi-step process involving: (a) treating a phenylhydrazine, or salt thereof, with a chloroformate; (b) adding phosgene; (c) treating the resulting product with an amine; and (d) hydrolyzing the resulting acylated semicarbazide. The reaction can proceed through a Δ2 -1,3,4-oxadiazolin-5-one intermediate formed with heating in step (b). Certain of the products are novel compounds.