(2R,6S)-4-(3-Fluoro-5-nitrophenyl)-2,6-dimethylmorpholine

96%

Reagent Code: #232132
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CAS Number 1955474-28-8

science Other reagents with same CAS 1955474-28-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.26 g/mol
Formula C₁₂H₁₅FN₂O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. The fluorine and nitro substituents on the phenyl ring enhance cell membrane permeability and biological target specificity, enabling the design of potent, low-dose therapeutics. The chiral morpholine core facilitates selective binding to protein targets in cell signaling pathways and optimization of pharmacokinetic properties, including absorption, distribution, and excretion. Commonly employed in medicinal chemistry to improve drug potency and metabolic stability. Also utilized in research to explore structure-activity relationships in heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,650.00
(2R,6S)-4-(3-Fluoro-5-nitrophenyl)-2,6-dimethylmorpholine
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. The fluorine and nitro substituents on the phenyl ring enhance cell membrane permeability and biological target specificity, enabling the design of potent, low-dose therapeutics. The chiral morpholine core facilitates selective binding to protein targets in cell signaling pathways and optimization of pharmacokinetic properties, including absorption, distribution, and excretion

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. The fluorine and nitro substituents on the phenyl ring enhance cell membrane permeability and biological target specificity, enabling the design of potent, low-dose therapeutics. The chiral morpholine core facilitates selective binding to protein targets in cell signaling pathways and optimization of pharmacokinetic properties, including absorption, distribution, and excretion. Commonly employed in medicinal chemistry to improve drug potency and metabolic stability. Also utilized in research to explore structure-activity relationships in heterocyclic compounds.

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