23448-86-4

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This describes the specific arrangement of atoms and bonds in the compound, which is a heterocyclic organic compound with a triazine ring structure and a phenyl group attached at the 6th position.
3. Heterocyclic Organic Compound

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements, in this case, carbon, nitrogen, and oxygen.
4. Triazine Ring Structure

Explanation

The compound features a triazine ring, which is a six-membered ring containing three nitrogen atoms and three carbon atoms.
5. 6-Phenyl Substitution

Explanation

A phenyl group (C6H5) is attached to the 6th position of the triazine ring, which influences the compound's characteristics and reactivity.
6. Applications in Pharmaceutical Synthesis

Explanation

The compound is used as a building block in the synthesis of various pharmaceuticals due to its unique structure and reactivity.
7. Applications in Agrochemical Research

Explanation

It is also utilized in the development of agrochemicals, which are chemicals used in the agricultural industry, such as pesticides and fertilizers.

Explanation

The compound exhibits these properties, making it potentially useful in the development of treatments for fungal and bacterial infections.
9. Building Block in Organic Synthesis and Medicinal Chemistry

Explanation

Due to its specific characteristics and reactivity, the compound serves as a valuable building block in the synthesis of various organic compounds and pharmaceuticals.
10. Potential Applications in Materials Science

Explanation

The compound may have uses in the development of new materials with unique properties, such as those with enhanced stability or reactivity.
11. Precursor for Derivatives with Diverse Properties and Uses

Explanation

The compound can be used as a starting material to synthesize a range of derivatives with different properties and potential applications in various fields.

Chemical Structure

1,2,4-Triazin-3(2H)-one, 6-phenyl-

Biological Activities

Antifungal and Antibacterial Properties

Upstream product

• 942-72-3 3-amino-6-phenyl-1,2,4-triazine 
• 73214-24-1 3-chloro-6-phenyl-1,2,4-triazine 
• 1075-06-5 2,2-dihydroxy-1-phenyl-ethanone 

Downstream Products

• 98454-67-2 5-(2-oxopropyl)-6-phenyl-4,5-dihydro-1,2,4-triazin-3(2H)-one 
• 98454-63-8 2-ethoxymethyl-5-phenyl-1,2,4-triazin-3(2H)-one 
• 73214-24-1 3-chloro-6-phenyl-1,2,4-triazine 
• 38119-46-9 5-Thioxo-6-phenyl-4,5-dihydro-1,2,4-triazin-3(2H)-one 
• 727664-17-7 6-phenyl-5-(thiophen-2-yl)-4,5-dihydro-1,2,4-triazin-3(2H)-one 
• 352214-70-1 5-[2-oxo-2-(thiophen-2-yl)ethyl]-6-phenyl-4,5-dihydro-1,2,4-triazin-3(2H)-one 
• 98454-68-3 2-benzyl-5-(2-oxopropyl)-6-phenyl-4,5-dihydro-1,2,4-triazin-3(2H)-one 
• 1355956-06-7 2-eethyl-5-(2-oxopropyl)-6-phenyl-4,5-dihydro-1,2,4-triazin-3(2H)-one 
• 1355956-10-3 5-(2-oxopropyl)-6-phenyl-2-propyl-4,5-dihydro-1,2,4-triazin-3(2H)-one 

Relevant academic research and scientific papers

Ring transformation of 3-halo-1,2,4-triazines with α-chlorocarbanions: A novel route to pyrazoles with sulfonyl, sulfonamido and sulfonyloxy groups

A novel route to pyrazoles bearing sulfonyl, sulfonamido and sulfonyloxy groups at C-3 by ring cleavage reaction of 3-halo-6-phenyl-1,2,4-triazines (1a-b) with α-halocarbanions (2a-g) is described.