5-Boc-4,5,6,7-tetrahydrofuro[3,2-c]pyridine

95%

Reagent Code: #173580
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CAS Number 179060-34-5

science Other reagents with same CAS 179060-34-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.27 g/mol
Formula C₁₂H₁₇NO₃
badge Registry Numbers
MDL Number MFCD22574995
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 central nervous system (CNS) agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to build drug candidates targeting neurological disorders and certain cancers. The Boc-protected amine group enables controlled deprotection and coupling reactions, facilitating efficient and selective synthesis routes in multi-step organic transformations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿36,310.00
inventory 250mg
10-20 days ฿11,020.00

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5-Boc-4,5,6,7-tetrahydrofuro[3,2-c]pyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and central nervous system (CNS) agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to build drug candidates targeting neurological disorders and certain cancers. The Boc-protected amine group enables controlled deprotection and coupling reacti

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and central nervous system (CNS) agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to build drug candidates targeting neurological disorders and certain cancers. The Boc-protected amine group enables controlled deprotection and coupling reactions, facilitating efficient and selective synthesis routes in multi-step organic transformations.

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