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495415-51-5

4-Trifluoromethyl-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester

Catalog#: AR00DMDU  |   CAS#: 495415-51-5  |   MDL#: MFCD11848173  |   MF: C12H18F3NO4  |   MW: 297.2708295999999

Packsize Purity Price Availability Quantity
50mg 97% $118.00 Global Stock Buy Now Add To Cart
100mg 97% $200.00 Global Stock Buy Now Add To Cart
250mg 97% $397.00 Global Stock Buy Now Add To Cart
1g 97% $984.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DMDU
Chemical Name 4-Trifluoromethyl-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester
CAS Number 495415-51-5
Molecular Formula C12H18F3NO4
Molecular Weight 297.2708295999999
MDL Number MFCD11848173
SMILES O=C(N1CCC(CC1)(C(=O)O)C(F)(F)F)OC(C)(C)C

1-(tert-Butoxycarbonyl)-4-(trifluoromethyl)piperidine-4-carboxylic acid is a versatile compound widely utilized in chemical synthesis for its unique properties and diverse applications. In organic synthesis, this compound serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its strategic incorporation in synthetic pathways facilitates the efficient construction of complex molecular structures, enabling the synthesis of biologically active compounds with enhanced pharmacological properties.This compound plays a crucial role as a protecting group in the synthesis of peptides and other organic molecules. By temporarily masking reactive functional groups, such as amines, the tert-butoxycarbonyl (Boc) moiety ensures selective reactivity and prevents unwanted side reactions during chemical transformations. Moreover, the presence of the trifluoromethyl group in the piperidine ring confers unique physicochemical properties to the final products, enhancing their biological activity and metabolic stability.Furthermore, 1-(tert-Butoxycarbonyl)-4-(trifluoromethyl)piperidine-4-carboxylic acid is employed in the development of new synthetic methodologies and cascade reactions. Its structural features enable the efficient construction of diverse chemical scaffolds through strategic bond formations and functional group manipulations. This compound's versatility and reactivity make it a valuable tool for synthetic chemists striving to access novel compounds and improve existing synthetic routes for complex molecule synthesis.
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