(S)-1-N-BOC-2-METHYL PIPERAZINE

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Reagent Code: #234626
label
Alias (S)-1-N-Boc-2-methylpiperazine; (S)-2-methylpiperazine-1-carboxylate tert-butyl; S-N-BOC-2-methylpiperazine;
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CAS Number 169447-70-5

science Other reagents with same CAS 169447-70-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.28 g/mol
Formula C₁₀H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD01862121
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected amine group allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, antimicrobial agents, and kinase inhibitors. The S-configuration enables specific interactions in biological systems, enhancing the efficacy and selectivity of the final drug compound.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿960.00
inventory 25g
10-20 days ฿4,450.00
inventory 100g
10-20 days ฿17,660.00

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(S)-1-N-BOC-2-METHYL PIPERAZINE
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected amine group allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, antimicrobial agents, and kinase inhibitors. The S-configuration enables specific inter

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected amine group allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, antimicrobial agents, and kinase inhibitors. The S-configuration enables specific interactions in biological systems, enhancing the efficacy and selectivity of the final drug compound.

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