4410-17-7

Basic information

• Product Name: 1-(2-(4-bromophenyl)ethylidene)-2-(2,4-dinitrophenyl)hydrazine
• Synonyms: 1-(2-(4-bromophenyl)ethylidene)-2-(2,4-dinitrophenyl)hydrazine
• CAS NO: 4410-17-7
• Molecular Weight: 379.17
• Mol File: 4410-17-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-(2-(4-bromophenyl)ethylidene)-2-(2,4-dinitrophenyl)hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-(4-bromophenyl)ethylidene)-2-(2,4-dinitrophenyl)hydrazine(4410-17-7)
• EPA Substance Registry System: 1-(2-(4-bromophenyl)ethylidene)-2-(2,4-dinitrophenyl)hydrazine(4410-17-7)

Safety Data

• Hazardous Substances Data: 4410-17-7(Hazardous Substances Data)

Upstream product

• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 1122-91-4 4-bromo-benzaldehyde 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 2028-85-5 (4-bromophenyl)diazonium chloride 
• 349647-31-0 1-Bromo-4-((E)-2-phenoxy-vinyl)-benzene 
• 111615-85-1 (E)-1-(2-butoxyethenyl)-4-bromobenzene 
• 132724-53-9 9-[1-Benzotriazol-1-yl-2-(4-bromo-phenyl)-ethyl]-9H-carbazole 

Relevant articles and documents

Hypoiodite-catalyzed regioselective oxidation of alkenes: An expeditious access to aldehydes in aqueous micellar media

A highly anti-Markovnikov selective oxidation of alkenes based on in situ generated hypoiodite catalysis in aqueous micellar media under mild conditions has been described. This novel catalytic system realizes an efficient synthesis of aldehydes from alkenes in an economically viable and environmentally safe fashion. The preliminary mechanistic studies suggest that the reaction proceeds via tandem iodofunctionalization/1,2-aryl or alkyl migration. The scope and limitations of this tandem process are demonstrated with various mono- and disubstituted (terminal and internal) olefins.

Diazo reactions with unsaturated compounds: V.1 reaction of phenyl vinyl ether with arenediazonium chlorides

Phenyl vinyl ether reacts with arenediazonium chlorides in aqueous acetone at pH 3-4 in the presence of a catalytic amount of copper(II) chloride to give arylacetaldehydes and small amounts 1-aryl-2-phenoxyethenes. No reaction occurs between the same reactants in the presence of sulfur(IV) oxide. 2000 MAIK "Nauka/Interperiodica".

1-(Carbazol-9-ylmethyl)benzotriazole Anion: A Formyl Anion Equivalent

The title anion, readily available as its lithium derivative, smoothly reacts with a wide range of electrophiles to give well-characterized products which are easily hydrolyzed to the corresponding aldehydes in high overall yields.The method is compared with currently available routes.