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(2Z)-4-Oxo-4-[3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-one
[CAS# 764667-65-4]

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Identification
Classification Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyrazines
Name (2Z)-4-Oxo-4-[3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-one
Synonyms (2Z)-1-[3-(Trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-yl]-4-(2,4,5-trifluorophenyl)butane-1,3-dione
Molecular Structure CAS # 764667-65-4, (2Z)-4-Oxo-4-[3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-one, (2Z)-1-[3-(Trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-yl]-4-(2,4,5-trifluorophenyl)butane-1,3-dione
Molecular Formula C16H12F6N4O2
Molecular Weight 406.28
CAS Registry Number 764667-65-4
EC Number 619-997-4
SMILES C1CN2C(=NN=C2C(F)(F)F)CN1C(=O)CC(=O)CC3=CC(=C(C=C3F)F)F
Properties
Density 1.6±0.1 g/cm3, Calc.*
Index of Refraction 1.58, Calc.*
Boiling Point 513.9±60.0 ºC (760 mmHg), Calc.*
Flash Point 264.6±32.9 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302-H315-H319-H335    Details
Precautionary Statements P261-P305+P351+P338    Details
SDS Available
up Discovory and Applicatios
The compound (2Z)-4-Oxo-4-[3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-one is a complex organic molecule that combines multiple functional groups and a significant degree of fluorination. It falls within the broader class of heterocyclic compounds, which are characterized by their incorporation of atoms like nitrogen and oxygen into their ring structures. This particular molecule contains a triazole ring, a pyrazine ring, and is heavily substituted with trifluoromethyl groups on the aromatic rings, making it a fluorinated heterocyclic compound.

The discovery and synthesis of compounds like this one, especially those containing both trifluoromethyl and heterocyclic moieties, have been an area of interest in medicinal and materials chemistry due to their potential for various bioactivities and their influence on the properties of organic materials. The trifluoromethyl group is known for enhancing the lipophilicity and metabolic stability of molecules, making such compounds valuable in the pharmaceutical industry.

In particular, fluorinated compounds like this one are often explored for their activity in drug discovery, especially as potential antifungal, antiviral, or anticancer agents, owing to the chemical stability imparted by the fluorine atoms. The presence of the triazole and pyrazine rings may suggest potential activity in areas related to enzyme inhibition or receptor binding, as these structural motifs are frequently observed in biologically active molecules.

Moreover, the chemical structure of this compound is highly specific and suggests that it could be used in the development of materials with unique electronic or optical properties, as well as in agricultural chemicals. For instance, compounds with fluorine atoms in specific positions are often studied for their utility as herbicides or pesticides due to their ability to interfere with biochemical pathways in plants or microbes.

Research into this molecule would typically focus on synthesizing it via well-established methods for creating fluorinated heterocycles and testing it in various biological assays to identify any pharmacological properties. Synthesis often involves reactions like nucleophilic substitution or condensation reactions to form the heterocyclic rings, followed by fluorination to introduce the trifluoromethyl groups.

Given the complexity of the structure, with both a triazole and pyrazine ring incorporated into the molecular backbone, the synthesis and study of this compound would contribute to the growing body of research in fluorinated heterocycles and their diverse applications in fields ranging from pharmaceuticals to agriculture and materials science.
Market Analysis Reports
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