tert-butyl N-[[2-(trifluoromethyl)pyridin-4-yl]methyl]carbamate


Chemical Name: tert-butyl N-[[2-(trifluoromethyl)pyridin-4-yl]methyl]carbamate
CAS Number: 916210-33-8
Product Number: AG006S6P(AGN-PC-0CXCHD)
Synonyms:
MDL No:
Molecular Formula: C12H15F3N2O2
Molecular Weight: 276.2549

Identification/Properties


Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The tert-Butyl ((2-(trifluoromethyl)pyridin-4-yl)methyl)carbamate is a versatile compound that plays a crucial role in chemical synthesis processes. This compound serves as a valuable building block in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and materials science. Its unique chemical structure, comprising a tertiary butyl group and a trifluoromethylpyridine moiety, provides opportunities for creating diverse chemical entities with enhanced properties.In chemical synthesis, tert-Butyl ((2-(trifluoromethyl)pyridin-4-yl)methyl)carbamate can act as a protecting group, shielding reactive functional groups from undesired reactions during synthetic pathways. By selectively modifying specific sites within complex molecules, this compound facilitates the efficient formation of desired products with high purity and yield. Additionally, its presence can influence the stereochemistry and reactivity of intermediates, allowing for precise control over reaction outcomes.Furthermore, tert-Butyl ((2-(trifluoromethyl)pyridin-4-yl)methyl)carbamate serves as a key intermediate in the synthesis of bioactive compounds and complex organic structures. Through strategic manipulation of its chemical reactivity, chemists can access a wide range of derivatives with tailored properties for various applications. This compound's compatibility with different reaction conditions and functional group transformations makes it a valuable tool for advancing synthetic methodologies and exploring new avenues in chemical design.