Ethyl 2-((tert-butoxycarbonyl)amino)-5-fluoro-2,3-dihydro-1H-indene-2-carboxylate

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Reagent Code: #180579
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CAS Number 1416440-28-2

science Other reagents with same CAS 1416440-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.35 g/mol
Formula C₁₇H₂₂NO₄F
badge Registry Numbers
MDL Number MFCD22689928
thermostat Physical Properties
Boiling Point 414.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated indene-based drugs. Its structure supports the construction of complex molecules with potential activity in central nervous system therapies and anti-inflammatory agents. The Boc-protected amine group allows for selective deprotection and further functionalization in multi-step organic syntheses. Commonly employed in medicinal chemistry for building blocks in drug discovery programs targeting kinase inhibitors and serotonin receptor modulators.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,400.00
inventory 1g
10-20 days ฿52,280.00

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Ethyl 2-((tert-butoxycarbonyl)amino)-5-fluoro-2,3-dihydro-1H-indene-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated indene-based drugs. Its structure supports the construction of complex molecules with potential activity in central nervous system therapies and anti-inflammatory agents. The Boc-protected amine group allows for selective deprotection and further functionalization in multi-step organic syntheses. Commonly employed in medicinal chemistry for building blocks in drug discovery programs target

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated indene-based drugs. Its structure supports the construction of complex molecules with potential activity in central nervous system therapies and anti-inflammatory agents. The Boc-protected amine group allows for selective deprotection and further functionalization in multi-step organic syntheses. Commonly employed in medicinal chemistry for building blocks in drug discovery programs targeting kinase inhibitors and serotonin receptor modulators.

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