(2R,5R)-tert-Butyl 5-(hydroxymethyl)-2-methylpiperazine-1-carboxylate

98%

Reagent Code: #230731
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CAS Number 1403898-64-5

science Other reagents with same CAS 1403898-64-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.3 g/mol
Formula C₁₁H₂₂N₂O₃
badge Registry Numbers
MDL Number MFCD28100885
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its stereochemistry enables selective interactions in biological systems, making it valuable for optimizing drug efficacy and metabolic stability. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the presence of functional groups amenable to further modification.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿830.00
inventory 100mg
10-20 days ฿1,310.00
inventory 250mg
10-20 days ฿3,110.00
inventory 1g
10-20 days ฿12,010.00
inventory 5g
10-20 days ฿42,000.00
(2R,5R)-tert-Butyl 5-(hydroxymethyl)-2-methylpiperazine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its stereochemistry enables selective interactions in biological systems, making it valuable for optimizing drug efficacy and metabolic stability. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the presence of functional groups amenable to further modification.

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its stereochemistry enables selective interactions in biological systems, making it valuable for optimizing drug efficacy and metabolic stability. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the presence of functional groups amenable to further modification.

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