5335-28-4

Basic information

• Product Name: (2E)-1-phenyl-2-(phenylhydrazono)ethanone
• Synonyms: (2E)-1-phenyl-2-(2-phenylhydrazinylidene)ethanone; benzeneacetaldehyde, α-oxo-, α-(2-phenylhydrazone)
• CAS NO: 5335-28-4
• Molecular Formula: C₁₄H₁₂N₂O
• Molecular Weight: 224.2579
• Mol File: 5335-28-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 366.1°C at 760 mmHg
• Flash Point: 175.2°C
• Density: 1.07g/cm³
• Vapor Pressure: 1.5E-05mmHg at 25°C
• Refractive Index: 1.578
• CAS DataBase Reference: (2E)-1-phenyl-2-(phenylhydrazono)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-1-phenyl-2-(phenylhydrazono)ethanone(5335-28-4)
• EPA Substance Registry System: (2E)-1-phenyl-2-(phenylhydrazono)ethanone(5335-28-4)

Safety Data

• Hazardous Substances Data: 5335-28-4(Hazardous Substances Data)

Usage

Description

(2E)-1-phenyl-2-(phenylhydrazono)ethanone, also known as benzophenone phenylhydrazone, is a hydrazone derivative with a molecular formula of C14H12N2O. It is characterized by its yellow color and belongs to the class of hydrazones, which are formed from hydrazine and aldehydes or ketones.

Uses

Used in Organic Synthesis:
(2E)-1-phenyl-2-(phenylhydrazono)ethanone is used as a reagent in organic synthesis for the formation of hydrazones, which are important intermediates in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
(2E)-1-phenyl-2-(phenylhydrazono)ethanone is used as a reactant in the preparation of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
(2E)-1-phenyl-2-(phenylhydrazono)ethanone is also used in the agrochemical industry for the preparation of agrochemicals, such as pesticides and herbicides, to improve crop protection and yield.
Used in Material Development:
(2E)-1-phenyl-2-(phenylhydrazono)ethanone has potential applications in the development of new materials, such as polymers and composites, due to its unique chemical properties.
Used in Biochemical Research:
(2E)-1-phenyl-2-(phenylhydrazono)ethanone is utilized in biochemical research for studying various biological processes and interactions, as well as for the development of new diagnostic and therapeutic tools.

Upstream product

• 40885-33-4 ethyl 2,3-dioxo-3-phenylpropanoate 2-phenylhydrazone 
• 614-20-0 3-oxo-3-phenylpropionic acid 
• 100-34-5 benzene diazonium chloride 
• 1074-12-0 phenylglyoxal hydrate 
• 59-88-1 phenylhydrazine hydrochloride 
• 532-54-7 oxo-phenyl-acetaldehyde oxime 
• 40885-73-2 (2Z)-3-oxo-3-phenyl-2-(2-phenylhydrazinylidene)propanoic acid 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 100-63-0 phenylhydrazine 
• 34885-34-2 phenyldiazonium acetate 

Downstream Products

• 744-25-2 2-Phenylhydrazono-3-piperidinopropiophenon 
• 33877-94-0 acetic acid-[(β-oxo-phenethylidene)-phenyl-hydrazide] 
• 107273-32-5 3-dimethylamino-1-phenyl-propane-1,2-dione-2-phenylhydrazone 
• 41270-75-1 4-phenyl-1H-imidazole-2-carboxamide 
• 304463-05-6 3-(4-benzyl-piperazin-1-yl)-1-phenyl-2-(phenyl-hydrazono)-propan-1-one 
• 110378-55-7 3-Morpholino-2-phenylhydrazonopropiophenon 
• 365276-42-2 3-(Perhydroazepin-1-yl)-2-phenylhydrazonopropiophenon 
• 94860-72-7 3-hydroxy-1-phenyl-2-(2-phenylhydrazono)propan-1-one 
• 1265802-06-9 3-amino-6-benzoyl-2,5-diphenyl-2,5-dihydropyridazine-4-carbonitrile 
• 1265802-12-7 3-amino-6-benzoyl-2,5-diphenyl-2,5-dihydropyridazine-4-carboxylic acid ethyl ester 
• 1265802-18-3 6-benzoyl-3-oxo-2,5-diphenyl-2,3-dihydropyridazine-4-carbonitrile 
• 121849-33-0 1,1'-diphenyl-3,3'-piperazine-1,4-diyl-bis-propane-1,2-dione 2,2'-bis-phenylhydrazone 
• 110378-55-7 3-morpholin-4-yl-1-phenyl-propane-1,2-dione 2-phenylhydrazone 
• 75872-31-0 6-Benzoyl-2,5-diphenyl-3(2H)-pyridazinon 

Relevant articles and documents

Pyrrolo[3,4-c]pyrazole Synthesis via Copper(?) Chloride-Catalyzed Oxidative Coupling of Hydrazones to Maleimides

A variety of pyrrolo[3,4-c]pyrazole derivatives from readily available aldehyde hydrazones and maleimides via direct oxidative coupling under radical cascade reaction have been reported. This method offers satisfactory chemical yields and good functional