Carbamic acid,[(1R)-3-[5,6-dihydro-3-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazin-7(8H)-yl]-3-oxo-1-[(2,4,5-trifluorophenyl)methyl]propyl]-, 1,1-dimethylethylester CAS:486460-23-5

The compound features a triazolo[4,3-a]pyrazin ring system, which is a fused heterocyclic compound consisting of a triazole and a pyrazine ring. This ring system is known for its stability and can exhibit unique electronic and chemical properties. The presence of the 5,6-dihydro group indicates that the ring system is partially reduced, which can affect its reactivity. The triazolo[4,3-a]pyrazin ring is further substituted with a trifluoromethyl group at the 3-position. Trifluoromethyl groups are known for their strong electron-withdrawing effect, which can influence the chemical reactivity of the compound. They are also commonly used in medicinal chemistry to modulate the pharmacokinetic and pharmacodynamic properties of molecules. The compound also features a carbamic acid ester group, which is a functional group consisting of a carbonyl group attached to an oxygen atom that is further attached to an alkyl or aryl group. In this case, the ester group is attached to a propyl chain, which is a three-carbon alkyl chain. Carbamic acid esters are commonly used as protecting groups in organic synthesis and can also be hydrolyzed to form the corresponding carboxylic acid. The 1,1-dimethylethyl ester group is a protecting group that protects the carbonyl oxygen atom of the carbamic acid from unwanted reactions. Protecting groups are commonly used in organic synthesis to allow for the sequential introduction of functional groups without interference from each other. The 2,4,5-trifluorophenyl group is an aromatic substituent that is attached to the propyl chain at the 1-position. This group contains three fluorine atoms, which contribute to the compound's overall polarity and can influence its solubility and reactivity. The (1R)-configuration indicates the absolute configuration of the molecule, which refers to the arrangement of the atoms in space. Absolute configuration is an important aspect of the biological activity of molecules, as it can determine how they interact with biological targets. Given its complex structure and the presence of multiple functional groups, the compound is likely to be of interest in organic synthesis and medicinal chemistry. It could be used as a building block for the synthesis of more complex molecules or could be further modified to explore its potential biological activity. The presence of the triazolo[4,3-a]pyrazin ring system and the triflu