(S)-1-(tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid

98%

Reagent Code: #233076
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CAS Number 1221793-42-5

science Other reagents with same CAS 1221793-42-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.25 g/mol
Formula C₁₁H₁₇F₂NO₄
badge Registry Numbers
MDL Number MFCD03094869
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and metabolic diseases. The (S)-configuration and 4,4-difluoro substitution provide high stereochemical purity and enhanced metabolic stability. Its carboxylic acid functionality supports the construction of complex molecules, while the Boc-protected piperidine scaffold improves stability and solubility during peptide-like synthesis, enabling efficient coupling reactions in multi-step organic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,890.00
inventory 250mg
10-20 days ฿22,160.00
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(S)-1-(tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and metabolic diseases. The (S)-configuration and 4,4-difluoro substitution provide high stereochemical purity and enhanced metabolic stability. Its carboxylic acid functionality supports the construction of complex molecules, while the Boc-protected piperidine scaffold improves stability and solubility during peptide-like synth

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and metabolic diseases. The (S)-configuration and 4,4-difluoro substitution provide high stereochemical purity and enhanced metabolic stability. Its carboxylic acid functionality supports the construction of complex molecules, while the Boc-protected piperidine scaffold improves stability and solubility during peptide-like synthesis, enabling efficient coupling reactions in multi-step organic routes.

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