6134-57-2

Basic information

• Product Name: Pentane-2,3,4-trione 3-phenylhydrazone
• Synonyms: 3-(2-Phenylhydrazono)-2,4-pentanedione;3-(2-Phenylhydrazono)pentane-2,4-dione;Pentane-2,3,4-trione 3-phenylhydrazone;3-(Phenyl-hydrazono)-pentane-2,4-dione
• CAS NO: 6134-57-2
• Molecular Formula: C₁₁H₁₂N₂O₂
• Molecular Weight: 0
• Mol File: 6134-57-2.mol
• Article Data: 24

Chemical Properties

• Boiling Point: 324°C at 760 mmHg
• Flash Point: 149.8°C
• Appearance: /
• Density: 1.11g/cm³
• Vapor Pressure: 0.000252mmHg at 25°C
• Refractive Index: 1.546
• CAS DataBase Reference: Pentane-2,3,4-trione 3-phenylhydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Pentane-2,3,4-trione 3-phenylhydrazone(6134-57-2)
• EPA Substance Registry System: Pentane-2,3,4-trione 3-phenylhydrazone(6134-57-2)

Safety Data

• Hazardous Substances Data: 6134-57-2(Hazardous Substances Data)

Usage

General Description

Pentane-2,3,4-trione 3-phenylhydrazone is a compound derived from the reaction of 2,3,4-pentanetrione and phenylhydrazine. It is a yellow crystalline solid with the molecular formula C12H12N2O. This chemical is commonly used in organic synthesis and as a reagent in the preparation of organic compounds. It has been found to exhibit potential biological activities, including antioxidant and antibacterial properties. Pentane-2,3,4-trione 3-phenylhydrazone is also used in research and development laboratories for its ability to form complexes with a variety of metal ions. Overall, this compound has diverse applications in chemical and biological sciences.

InChI:InChI=1/C11H12N2O2/c1-8(14)11(9(2)15)13-12-10-6-4-3-5-7-10/h3-7,12H,1-2H3

Upstream product

• 62-53-3 aniline 
• 123-54-6 acetylacetone 
• 7647-01-0 hydrogenchloride 
• 3762-55-8 3-phenylhydrazono-4-imino-2-pentanone 
• 100-34-5 benzene diazonium chloride 
• 15435-71-9 sodium acetylacetonate 

Downstream Products

• 5335-37-5 3-acetyl-1,5-diphenylformazan 
• 24756-09-0 3-(2-(4-bromophenyl)hydrazineylidene) pentane-2,4-dione 
• 99841-05-1 4-hydroxy-pentane-2,3-dione-3-phenylhydrazone 
• 70826-56-1 1-(4,6-dimethylpyrimidin-2-yl)-3,5-dimethyl-4-phenyl-azopyrazole 
• 75872-28-5 6-acetyl-5-methyl-2-phenylpyridazin-3(2H)-one 
• 140935-37-1 6-Acetyl-4-chloro-5-methyl-2-phenyl-2H-pyridazin-3-one 
• 140935-33-7 3-(N-Chloracetyl-N-phenylhydrazono)pentan-2,4-dion 
• 100621-53-2 2-mercapto-4,6-dimethyl-5-phenylazopyridine-3-carbonitrile 
• 37055-56-4 3,3-dibromo-N'-(2,4-dibromo-phenyl)-pyruvohydrazonoyl bromide 
• 5272-86-6 4-amino-3,5-dimethyl-1H-pyrazole 

Relevant articles and documents

Reversible switching of arylazopyrazole within a metal-organic cage

Arylazopyrazoles represent a new family of molecular photoswitches characterized by a near-quantitative conversion between two states and long thermal half-lives of the metastable state. Here, we investigated the behavior of a model arylazopyrazole in the

Chemoproteomics-Enabled De Novo Discovery of Photoswitchable Carboxylesterase Inhibitors for Optically Controlled Drug Metabolism

Herein, we report arylazopyrazole ureas and sulfones as a novel class of photoswitchable serine hydrolase inhibitors and present a chemoproteomic platform for rapid discovery of optically controlled serine hydrolase targets in complex proteomes. Specifica

Mixed isatin with 3-(2-(aryl)hydrazono)acetylacetone mn(ii), co(ii) and ni(ii) complexes: Antibacterial evaluation and molecular properties prediction

The metal complexes {Ni (II), Co (II) and Mn (II)} of 3-(2-(aryl)hydrazono)acetylacetone with isatin were synthesized and screened for their in vitro antibacterial activity against four pathogenic microorganisms {two Gram-positive and two Gram negative}.