74367-79-6

Usage

Common Uses

Organic chemistry, Analytical chemistry

Type of Compound

Derivative of hydrazinecarboxamide

Functional Group

Dinitrophenyl group

Reactivity

Reacts with aldehydes and ketones to form brightly colored derivatives

Specificity

Useful in qualitative and quantitative analysis of carbonyl compounds

Importance

Valuable tool in organic synthesis and chemical research

Upstream product

• 64-17-5 ethanol 
• 127-09-3 sodium acetate 
• 4426-72-6 hydrazine carboxamide 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 563-41-7 semicarbazide hydrochloride 
• 298-06-6 O,O-Diethyl hydrogen phosphorodithioate 
• 179807-92-2 4-chloroacetyl-1-(2',4'-dinitrophenyl)semicarbazide 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 

Relevant academic research and scientific papers

Synthesis of new organophosphorus derivatives of acylureas and acylsemicarbazides

A convenient route to phosphorus acylureas and acylsemicarbazides is reported. The syntheses of the new compounds involve the reaction between a chloroacetyl compound and various phosphorus starting materials (dithiophosphate, phosphine, phosphite and phosphinite).

Nucleophilic Reactivity: Nucleophilic Aromatic Substitution Reactions of 2,4-Dinitrochlorobenzene and Picryl Chloride in Aqueous and Methanol Solutions

Rate constants for nucleophilic aromatic substitution reactions of picryl chloride, I, with acetate ion and a series of amine nucleophiles, including primary, secondary, tertiary (quinuclidines), and amines which show the α-effect, in aqueous and methanol