940-54-5

Basic information

• Product Name: (1E)-1-butylidene-2-phenylhydrazine
• Synonyms: Butyraldehyde, phenylhydrazone
• CAS NO: 940-54-5
• Molecular Formula: C₁₀H₁₄N₂
• Molecular Weight: 162.2316
• Mol File: 940-54-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 264.168°C at 760 mmHg
• Flash Point: 113.565°C
• Density: 0.935g/cm³
• Vapor Pressure: 0.01mmHg at 25°C
• Refractive Index: 1.511
• CAS DataBase Reference: (1E)-1-butylidene-2-phenylhydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: (1E)-1-butylidene-2-phenylhydrazine(940-54-5)
• EPA Substance Registry System: (1E)-1-butylidene-2-phenylhydrazine(940-54-5)

Safety Data

• Hazardous Substances Data: 940-54-5(Hazardous Substances Data)

Usage

General Description

(1E)-1-butylidene-2-phenylhydrazine is an organic chemical compound with the molecular formula C12H16N2. It is used in the production of pharmaceuticals and agrochemicals, and it has also been studied for its potential use in the treatment of various diseases and medical conditions. (1E)-1-butylidene-2-phenylhydrazine has a butyl side chain attached to a hydrazine group, and a phenyl group attached to the nitrogen atom. It has been found to exhibit various biological activities, including anti-inflammatory, antioxidant, and anti-tumor properties. Additionally, it has been investigated for its potential as a pesticide and for its insecticidal and fungicidal properties. Overall, (1E)-1-butylidene-2-phenylhydrazine is a versatile chemical with a range of potential applications in the fields of medicine, agriculture, and industry.

Upstream product

• 540-63-6 ethane-1,2-dithiol 
• 123-72-8 butyraldehyde 
• 100-63-0 phenylhydrazine 
• 99167-08-5 N-butyl-N'-phenylhydrazine 

Downstream Products

• 957188-41-9 1-phenyl-3-propyl-5-trifluoromethyl-1H-pyrazole 
• 83637-23-4 2-sec-butyl-cyclohexylamine 
• 4632-01-3 2-sec.-butylcyclohexanol 
• 127680-03-9 ((Z)-But-1-enyl)-phenyl-diazene 
• 74327-71-2 but-1-enyl-phenyl-diazene 
• 81323-29-7 N-Phenyl-N'-1-aminobutylhydrazine 
• 861598-53-0 (E)-2-butylidene-1,1-diphenylhydrazine 
• 1484-19-1 3-ethyl-1H-indole 
• 111-92-2 dibutylamine 
• 109-73-9 N-butylamine 
• 62-53-3 aniline 
• 123-72-8 butyraldehyde 
• 115591-30-5 5-Methyl-1-phenyl-3-propyl-1H-[1,2,4]triazole 
• 74830-05-0 4-phenyl-5-phenylimino-2-propyl-1,3,4-thiadiazolidine 

Relevant articles and documents

Dehydrogenation of 1-(diphenylphosphinoyl)-2-(N′-phenylhydrazino) ethane and N-butyl-N′-phenylhydrazine

Dehydrogenation of 1-(diphenylphosphinoyl)-2-hydrazino-substituted ethanes and N-butyl-N′-phenylhydrazine to the corresponding hydrazone derivatives is performed. Both reactions were established to involve predominantly, if not exclusively, an azo interme

Fast hydrazone reactants: Electronic and acid/base effects strongly influence rate at biological pH

Kinetics studies with structurally varied aldehydes and ketones in aqueous buffer at pH 7.4 reveal that carbonyl compounds with neighboring acid/base groups form hydrazones at accelerated rates. Similarly, tests of a hydrazine with a neighboring carboxylic acid group show that it also reacts at an accelerated rate. Rate constants for the fastest carbonyl/hydrazine combinations are 2-20 M-1 s-1, which is faster than recent strain-promoted cycloaddition reactions.

Synthesis of 3-ethyl indole

In this study, it is planned to synthesize intermediates to get β-carboline alkaloids having effective bioligical activities. In this way, we tried to synthesize 3-ethyl indole as an intermediate from simple and cheap compounds to obtain the β-carboline s