6024-59-5

Basic information

• Product Name: 2-[(3,5-dimethoxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]hydrazinecarboxamide
• CAS NO: 6024-59-5
• Molecular Formula: C₁₀H₁₃N₃O₄
• Molecular Weight: 239.2279
• Mol File: 6024-59-5.mol
• Article Data: 3

Chemical Properties

• Density: 1.32g/cm³
• Refractive Index: 1.578
• CAS DataBase Reference: 2-[(3,5-dimethoxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]hydrazinecarboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(3,5-dimethoxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]hydrazinecarboxamide(6024-59-5)
• EPA Substance Registry System: 2-[(3,5-dimethoxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]hydrazinecarboxamide(6024-59-5)

Safety Data

• Hazardous Substances Data: 6024-59-5(Hazardous Substances Data)

Usage

Molecular structure

2-[(3,5-dimethoxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]hydrazinecarboxamide has a complex molecular structure, which includes a hydrazinecarboxamide group, a cyclohexa-2,5-dien-1-ylidene)methyl group, methoxy and oxo substituents.

Potential applications

This chemical compound may have potential applications in pharmaceuticals or organic synthesis due to its unique structure.

Further study required

It would require further study and evaluation to determine the specific properties and potential uses of 2-[(3,5-dimethoxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]hydrazinecarboxamide.

Complex nature

The complex nature of the compound suggests that it may have specific reactivity or functionality.

Interest to researchers

The compound's unique structure and potential reactivity or functionality could be of interest to researchers in the chemical or pharmaceutical industries.

Upstream product

• 79-19-6 thiosemicarbazide 
• 134-96-3 syringic aldehyde 
• 563-41-7 semicarbazide hydrochloride 
• 39657-47-1 O-acetylsyringic acid chloride 

Downstream Products

• 1308789-42-5 2-amino-5-(3,5-dimethoxy-4-hydroxyphenyl)-1,3,4-oxadiazole 
• 1491167-93-1 C₁₅H₁₅N₃O₆S 

Relevant articles and documents

Synthesis of nitrogenated lignin-derived compounds and reactivity with laccases. Study of their application in mild chemoenzymatic oxidative processes

The chemical synthesis of a series of lignin-derived nitrogenated compounds was performed in high yields (73-99%) through simple conventional chemical transformations starting from natural monomers such as vanillin, syringaldehyde or 3,4-dihydroxybenzaldehyde. The study of the vanillin-derived compounds as substrates for commercially available laccases from Trametes versicolor and Myceliophthora thermophila in oxidative transformations, generally led to the isolation of several dimeric species in high to excellent conversions (>70%), while for hydrazone derivatives a more rapidly oxidative coupling was evidenced by the formation of oligomers and/or polymers. Remarkably, vanillin was obtained due to the hydrolysis of some of the nitrogenated functional groups, such as the hydrazone or the hydrazono tetrazole. The three families of lignin-derived compounds can provide a great source of new laccase-mediator systems (LMS), the possibility of employing them for lignin modification being particularly attractive. Preliminary experiments showed promising levels of activity towards the oxidation of a monomer (veratryl alcohol, up to 70% conversion) and a dimer (adlerol, up to 22% conversion) lignin models, higher than those achieved with the natural vanillin and syringaldehyde (up to 7% conversion with veratryl alcohol and almost negligible conversion with adlerol), these processes being also highly influenced by the pH of the reaction medium.

Synthesis and biological activity of 5-substituted-2-amino-1,3,4-oxadiazole derivatives

Electrical energy offers numerous benefits for performing synthesis, including increased reaction rates, enhanced yields, and cleaner chemistries. 5-Substituted-2-amino-1,3,4-oxadiazoles were synthesized directly from the semicarbazone at a platinum elect