(S)-Tert-Butyl 1-Hydroxyhexan-2-Ylcarbamate

95%

Reagent Code: #237130
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CAS Number 116640-16-5

science Other reagents with same CAS 116640-16-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.31 g/mol
Formula C₁₁H₂₃NO₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors and other bioactive molecules. Its hydroxyl and carbamate functional groups allow for selective chemical modifications, making it valuable in asymmetric synthesis. Commonly employed in the development of antiviral and anticancer agents where stereochemistry plays a critical role in biological activity. The compound’s structure supports peptide mimetic design, enabling enhanced metabolic stability and binding affinity in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,340.00
inventory 250mg
10-20 days ฿39,930.00
inventory 1g
10-20 days ฿66,390.00
(S)-Tert-Butyl 1-Hydroxyhexan-2-Ylcarbamate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors and other bioactive molecules. Its hydroxyl and carbamate functional groups allow for selective chemical modifications, making it valuable in asymmetric synthesis. Commonly employed in the development of antiviral and anticancer agents where stereochemistry plays a critical role in biological activity. The compound’s structure supports peptide mimetic design, enabling enhanced metaboli

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors and other bioactive molecules. Its hydroxyl and carbamate functional groups allow for selective chemical modifications, making it valuable in asymmetric synthesis. Commonly employed in the development of antiviral and anticancer agents where stereochemistry plays a critical role in biological activity. The compound’s structure supports peptide mimetic design, enabling enhanced metabolic stability and binding affinity in drug candidates.

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