Morpholino(quinoxalin-6-yl)methanone

≥95%

Reagent Code: #205514
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CAS Number 312319-71-4

science Other reagents with same CAS 312319-71-4

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Weight 243.26 g/mol
Formula C₁₃H₁₃N₃O₂
badge Registry Numbers
MDL Number MFCD01444315
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly those targeting cancer pathways. Its structure supports binding to ATP sites in kinases, making it valuable in developing anticancer agents. Also explored in medicinal chemistry for optimizing drug candidates due to its favorable solubility and stability properties. Shows potential in creating derivatives with antimicrobial and antiviral activities. Employed in structure-activity relationship (SAR) studies to enhance potency and selectivity of bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,950.00
inventory 250mg
10-20 days ฿6,990.00
inventory 1g
10-20 days ฿18,950.00

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Morpholino(quinoxalin-6-yl)methanone
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly those targeting cancer pathways. Its structure supports binding to ATP sites in kinases, making it valuable in developing anticancer agents. Also explored in medicinal chemistry for optimizing drug candidates due to its favorable solubility and stability properties. Shows potential in creating derivatives with antimicrobial and antiviral activities. Employed in structure-activity relationship (SAR) s

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly those targeting cancer pathways. Its structure supports binding to ATP sites in kinases, making it valuable in developing anticancer agents. Also explored in medicinal chemistry for optimizing drug candidates due to its favorable solubility and stability properties. Shows potential in creating derivatives with antimicrobial and antiviral activities. Employed in structure-activity relationship (SAR) studies to enhance potency and selectivity of bioactive molecules.

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