cis-5-Boc-1H-Hexahydropyrrolo[3,4-b]pyrrole

≥97%

Reagent Code: #173501
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CAS Number 180975-51-3

science Other reagents with same CAS 180975-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.29 g/mol
Formula C₁₁H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD11045908
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its rigid, fused bicyclic structure with defined stereochemistry makes it valuable for designing drugs targeting central nervous system disorders and metabolic diseases. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses, enhancing its utility in medicinal chemistry. Commonly employed in research settings for scaffold diversification in high-throughput drug discovery programs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿19,540.00
inventory 5g
10-20 days ฿73,500.00

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cis-5-Boc-1H-Hexahydropyrrolo[3,4-b]pyrrole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its rigid, fused bicyclic structure with defined stereochemistry makes it valuable for designing drugs targeting central nervous system disorders and metabolic diseases. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses, enhancing its utility in medicinal chemistry. Commonly empl

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its rigid, fused bicyclic structure with defined stereochemistry makes it valuable for designing drugs targeting central nervous system disorders and metabolic diseases. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses, enhancing its utility in medicinal chemistry. Commonly employed in research settings for scaffold diversification in high-throughput drug discovery programs.

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