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Structure of 188975-15-7
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Tert-butyl 4-(4-amino-2-fluorophenyl)piperidine-1-carboxylate features a fluorinated aromatic ring paired with a piperidine scaffold, enabling integration into bioactive molecules requiring enhanced metabolic stability and membrane permeability. The tert-butyl ester group offers convenient protection for the carboxylic acid functionality during synthetic manipulations. This intermediate supports efficient access to kinase inhibitors and CNS-targeted pharmaceuticals through straightforward deprotection and functionalization.
Tert-butyl 4-(4-amino-2-fluorophenyl)piperidine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted piperidine scaffolds. The ortho-fluoro substituent enhances metabolic stability and modulates electronic properties, while the tert-butyl carbamate group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. This compound functions effectively in standard coupling reactions and supports the construction of complex heterocyclic systems relevant to kinase inhibitors and CNS-targeted therapeutics.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: