4-[(3-Chloro-quinoxalin-2-ylamino)-methyl]-piperidine-1-carboxylicacidtert-butylester

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Reagent Code: #164394
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CAS Number 939986-05-7

science Other reagents with same CAS 939986-05-7

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scatter_plot Molecular Information
Weight 376.88 g/mol
Formula C₁₉H₂₅ClN₄O₂
badge Registry Numbers
MDL Number MFCD09607513
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing kinase inhibitors, particularly in the development of anticancer agents. Its structure, featuring a quinoxaline core linked to a piperidine ring with Boc protection, supports binding to specific enzyme targets involved in cell signaling pathways. Commonly employed in medicinal chemistry for optimizing drug candidates due to its favorable solubility and stability properties. Also utilized in the preparation of bioactive molecules targeting inflammatory and proliferative diseases.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿18,540.00

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4-[(3-Chloro-quinoxalin-2-ylamino)-methyl]-piperidine-1-carboxylicacidtert-butylester
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Used in pharmaceutical research as an intermediate for synthesizing kinase inhibitors, particularly in the development of anticancer agents. Its structure, featuring a quinoxaline core linked to a piperidine ring with Boc protection, supports binding to specific enzyme targets involved in cell signaling pathways. Commonly employed in medicinal chemistry for optimizing drug candidates due to its favorable solubility and stability properties. Also utilized in the preparation of bioactive molecules targetin

Used in pharmaceutical research as an intermediate for synthesizing kinase inhibitors, particularly in the development of anticancer agents. Its structure, featuring a quinoxaline core linked to a piperidine ring with Boc protection, supports binding to specific enzyme targets involved in cell signaling pathways. Commonly employed in medicinal chemistry for optimizing drug candidates due to its favorable solubility and stability properties. Also utilized in the preparation of bioactive molecules targeting inflammatory and proliferative diseases.

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