Tert-butyl 4-(trifluoromethyl)-2-formylphenylcarbamate, identified by its CAS number 212696-38-3, is a chemical compound that features a tert-butyl group, a trifluoromethyl substituent, and a carbamate functional group. This compound is characterized by its relatively complex structure, which includes an aromatic ring with both electron-withdrawing and electron-donating groups, influencing its reactivity and solubility. The presence of the trifluoromethyl group typically enhances the compound's lipophilicity and can affect its biological activity, making it of interest in medicinal chemistry and agrochemical applications. The carbamate moiety suggests potential for interactions with biological systems, as carbamates are known for their roles in enzyme inhibition and as intermediates in various synthetic pathways. Additionally, the compound's stability and reactivity can be influenced by the steric hindrance provided by the tert-butyl group. Overall, this compound's unique characteristics make it a subject of interest for further research in various chemical and pharmaceutical contexts.

tert-butyl 4-(trifluoroMethyl)-2-forMylphenylcarbaMate

212696-38-3: Tert-butyl 4-(trifluoromethyl)-2-formylphenylcarbamate, identified by its CAS number 212696-38-3, is a chemical compound that features a tert-butyl group, a trifluoromethyl substituent, and a carbamate functional group. This compound is characterized by its relatively complex structure, which includes an aromatic ring with both electron-withdrawing and electron-donating groups, influencing its reactivity and solubility. The presence of the trifluoromethyl group typically enhances the compound's lipophilicity and can affect its biological activity, making it of interest in medicinal chemistry and agrochemical applications. The carbamate moiety suggests potential for interactions with biological systems, as carbamates are known for their roles in enzyme inhibition and as intermediates in various synthetic pathways. Additionally, the compound's stability and reactivity can be influenced by the steric hindrance provided by the tert-butyl group. Overall, this compound's unique characteristics make it a subject of interest for further research in various chemical and pharmaceutical contexts.

Tert-butyl (2-formyl-4-(trifluoromethyl)phenyl)carbamate

CAS 212696-38-3

tert-butyl 4-(trifluoroMethyl)-2-forMylphenylcarbaMate

Tert-butyl (2-formyl-4-(trifluoromethyl)phenyl)carbamate

Ref: 54-PC109642

Tert-butyl (2-formyl-4-(trifluoromethyl)phenyl)carbamate

Ref: 10-F731191