N-(4-Bromo-3-Fluorobenzyl)Morpholine

97%

Reagent Code: #220086
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CAS Number 897016-96-5

science Other reagents with same CAS 897016-96-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.13 g/mol
Formula C₁₁H₁₃BrFNO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Also employed in the preparation of bioactive molecules in medicinal chemistry research due to its halogenated aromatic core and amine functionality. The compound's stability and reactivity make it suitable for coupling reactions in multi-step organic syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,200.00
500mg
10-20 days ฿7,490.00
1g
10-20 days ฿9,970.00
250mg
10-20 days ฿4,410.00
5g
10-20 days ฿29,110.00

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N-(4-Bromo-3-Fluorobenzyl)Morpholine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Also employed in the preparation of bioactive molecules in medicinal chemistry research due to its halogenated aromatic core and amine functionality. The compound's stability and reactivity make it suitable for coupling reactions in multi-step organic syntheses.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Also employed in the preparation of bioactive molecules in medicinal chemistry research due to its halogenated aromatic core and amine functionality. The compound's stability and reactivity make it suitable for coupling reactions in multi-step organic syntheses.

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