(S)-2-Boc-aminoethyl-piperidine

≥95%

Reagent Code: #235895
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CAS Number 1821799-30-7

science Other reagents with same CAS 1821799-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.33 g/mol
Formula C₁₂H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD28165868
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed, inflatable

description Product Description

Used in pharmaceutical synthesis as a chiral building block for the development of bioactive molecules. Its protected amine group allows for selective deprotection and coupling in peptide-like structures, making it valuable in the design of protease inhibitors and receptor ligands. Commonly employed in the preparation of drug candidates targeting central nervous system disorders due to the piperidine moiety’s prevalence in neuroactive compounds. The (S)-configuration enables stereocontrolled synthesis, enhancing potency and selectivity in final active ingredients.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,580.00
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(S)-2-Boc-aminoethyl-piperidine
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Used in pharmaceutical synthesis as a chiral building block for the development of bioactive molecules. Its protected amine group allows for selective deprotection and coupling in peptide-like structures, making it valuable in the design of protease inhibitors and receptor ligands. Commonly employed in the preparation of drug candidates targeting central nervous system disorders due to the piperidine moiety’s prevalence in neuroactive compounds. The (S)-configuration enables stereocontrolled synthesis, e

Used in pharmaceutical synthesis as a chiral building block for the development of bioactive molecules. Its protected amine group allows for selective deprotection and coupling in peptide-like structures, making it valuable in the design of protease inhibitors and receptor ligands. Commonly employed in the preparation of drug candidates targeting central nervous system disorders due to the piperidine moiety’s prevalence in neuroactive compounds. The (S)-configuration enables stereocontrolled synthesis, enhancing potency and selectivity in final active ingredients.

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