82511-80-6

Basic information

• Product Name: 1-[4-methyl-2-oxo-1-(prop-1-en-2-yl)cyclohex-3-en-1-yl]-4-phenyl-1,2,4-triazolidine-3,5-dione
• CAS NO: 82511-80-6
• Molecular Formula: C₁₈H₁₉N₃O₃
• Molecular Weight: 325.3618
• Mol File: 82511-80-6.mol
• Article Data: 2

Chemical Properties

• Density: 1.271g/cm³
• Refractive Index: 1.602
• CAS DataBase Reference: 1-[4-methyl-2-oxo-1-(prop-1-en-2-yl)cyclohex-3-en-1-yl]-4-phenyl-1,2,4-triazolidine-3,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[4-methyl-2-oxo-1-(prop-1-en-2-yl)cyclohex-3-en-1-yl]-4-phenyl-1,2,4-triazolidine-3,5-dione(82511-80-6)
• EPA Substance Registry System: 1-[4-methyl-2-oxo-1-(prop-1-en-2-yl)cyclohex-3-en-1-yl]-4-phenyl-1,2,4-triazolidine-3,5-dione(82511-80-6)

Safety Data

• Hazardous Substances Data: 82511-80-6(Hazardous Substances Data)

Usage

Explanation

The compound's full chemical name, which describes its structure and composition.

Explanation

A shorter, more common name used to refer to the compound.

Explanation

The compound belongs to a specific class of chemical compounds, which are characterized by their triazolodione structure.

Explanation

Tebufelone is classified as an NSAID, which means it is used to reduce inflammation, pain, and fever.

Explanation

The compound works by inhibiting the activity of cyclooxygenase enzymes, which are involved in the synthesis of prostaglandins, leading to reduced inflammation, pain, and fever.

Explanation

Tebufelone has been studied for its potential use in treating conditions like arthritis due to its anti-inflammatory properties.

Explanation

Tebufelone has also been investigated for its potential in the field of oncology, as it may have anti-cancer and anti-tumor effects.

Explanation

The compound is of interest to researchers in the fields of medicinal chemistry and pharmacology due to its potential therapeutic applications and unique chemical structure.

Class

Triazolodione derivatives

Type

Non-steroidal anti-inflammatory drug (NSAID)

Mechanism of Action

Inhibition of cyclooxygenase enzymes

Potential Applications

Treatment of inflammatory and painful conditions, such as arthritis

Additional Studies

Anti-cancer and anti-tumor properties

Field of Interest

Medicinal chemistry and pharmacology

Upstream product

• 4233-33-4 4-Phenyl-1,2,4-triazolidine-3,5-dione 
• 491-09-8 3-terpinolenone 
• 15988-11-1 4-Phenylurazole 

Relevant articles and documents

Reaction of Some Compounds Having Both Endo and Exo Olefinic Bonds with 1,2,4-Triazoline-3,5-diones

Reaction of piperitenone, (+)-limonene, or styrene with 1,2,4-triazoline-3,5-dione (TAD) produces adducts by ene reaction.The reaction of (+)-limonene gives a 2:1 adduct which results from further addition of TAD to an intermediary ene reaction product.Th