(5S,8S,10aR)-Methyl5-((tert-butoxycarbonyl)amino)-6-oxodecahydropyrrolo[1,2-a][1,5]diazocine-8-carboxylate

98%

Reagent Code: #237543
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CAS Number 957135-12-5

science Other reagents with same CAS 957135-12-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.4 g/mol
Formula C₁₆H₂₇N₃O₅
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of complex pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports the construction of peptidomimetics, enabling enhanced metabolic stability and improved binding affinity to target enzymes. Commonly employed in medicinal chemistry for optimizing drug candidates, especially in antiviral and anticancer research. The presence of protected functional groups allows selective modifications, making it valuable in multi-step organic syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿6,820.00
100mg
10-20 days ฿10,220.00
250mg
10-20 days ฿17,030.00
1g
10-20 days ฿36,400.00
(5S,8S,10aR)-Methyl5-((tert-butoxycarbonyl)amino)-6-oxodecahydropyrrolo[1,2-a][1,5]diazocine-8-carboxylate
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Used as a key intermediate in the synthesis of complex pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports the construction of peptidomimetics, enabling enhanced metabolic stability and improved binding affinity to target enzymes. Commonly employed in medicinal chemistry for optimizing drug candidates, especially in antiviral and anticancer research. The presence of protected functional groups allows selective modifications, making

Used as a key intermediate in the synthesis of complex pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports the construction of peptidomimetics, enabling enhanced metabolic stability and improved binding affinity to target enzymes. Commonly employed in medicinal chemistry for optimizing drug candidates, especially in antiviral and anticancer research. The presence of protected functional groups allows selective modifications, making it valuable in multi-step organic syntheses.

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