tert-butyl((2S)-1-hydroxy-3-(2-oxopyrrolidin-3-yl)propan-2-yl)carbamate

97%

Reagent Code: #237563
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CAS Number 2382782-88-7

science Other reagents with same CAS 2382782-88-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.32 g/mol
Formula C₁₂H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD31630889
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of neuroactive drugs. Its structure, featuring a tert-butyl carbamate (Boc) protecting group on the amine functionality, supports the creation of chiral building blocks essential for drug candidates targeting central nervous system disorders. The Boc group allows for selective protection during synthesis and easy deprotection afterward. Commonly employed in research settings for designing protease inhibitors and cognitive enhancers. Also utilized in the preparation of nootropic agents due to its compatibility with pyrrolidone-based active ingredients.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿19,730.00
tert-butyl((2S)-1-hydroxy-3-(2-oxopyrrolidin-3-yl)propan-2-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of neuroactive drugs. Its structure, featuring a tert-butyl carbamate (Boc) protecting group on the amine functionality, supports the creation of chiral building blocks essential for drug candidates targeting central nervous system disorders. The Boc group allows for selective protection during synthesis and easy deprotection afterward. Commonly employed in research settings for designing protease inhibitor
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of neuroactive drugs. Its structure, featuring a tert-butyl carbamate (Boc) protecting group on the amine functionality, supports the creation of chiral building blocks essential for drug candidates targeting central nervous system disorders. The Boc group allows for selective protection during synthesis and easy deprotection afterward. Commonly employed in research settings for designing protease inhibitors and cognitive enhancers. Also utilized in the preparation of nootropic agents due to its compatibility with pyrrolidone-based active ingredients.
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