N-benzyloxycarbonyl-3-fluoro-4-morpholinoaniline

98%

Reagent Code: #217025
label
Alias (3-Fluoro-4-morpholinophenyl)benzyl carbamate
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CAS Number 168828-81-7

science Other reagents with same CAS 168828-81-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.36 g/mol
Formula C₁₈H₁₉FN₂O₃
badge Registry Numbers
MDL Number MFCD06658240
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports the construction of bioactive molecules with potential applications in cancer therapy and inflammatory diseases. The presence of the fluoro and morpholino groups enhances binding selectivity and metabolic stability in final drug candidates. Commonly employed in peptide coupling reactions and solid-phase synthesis due to the protecting group compatibility of the benzyloxycarbonyl moiety.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿270.00
inventory 100g
10-20 days ฿2,390.00
inventory 500g
10-20 days ฿11,810.00
inventory 25g
10-20 days ฿680.00

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N-benzyloxycarbonyl-3-fluoro-4-morpholinoaniline
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports the construction of bioactive molecules with potential applications in cancer therapy and inflammatory diseases. The presence of the fluoro and morpholino groups enhances binding selectivity and metabolic stability in final drug candidates. Commonly employed in peptide coupling reactions and solid-phase synthesis due to the protecting group compatibility of th

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports the construction of bioactive molecules with potential applications in cancer therapy and inflammatory diseases. The presence of the fluoro and morpholino groups enhances binding selectivity and metabolic stability in final drug candidates. Commonly employed in peptide coupling reactions and solid-phase synthesis due to the protecting group compatibility of the benzyloxycarbonyl moiety.

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