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

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Reagent Code: #164296
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CAS Number 939986-89-7

science Other reagents with same CAS 939986-89-7

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scatter_plot Molecular Information
Weight 362.854 g/mol
Formula C₁₈H₂₃ClN₄O₂
badge Registry Numbers
MDL Number MFCD09607863
inventory_2 Storage & Handling
Density 1.286 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as an intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell proliferation. Its structure supports the development of compounds with high selectivity and binding affinity to specific enzyme sites. Commonly utilized in medicinal chemistry for optimizing drug candidates in oncology and inflammatory disease programs. Suitable for solid-phase and solution-phase peptide-like synthesis due to the protected piperidine and carboxylic acid functionalities.

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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)-piperidine-1-carboxylicacidtert-butylester
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Used in pharmaceutical research as an intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell proliferation. Its structure supports the development of compounds with high selectivity and binding affinity to specific enzyme sites. Commonly utilized in medicinal chemistry for optimizing drug candidates in oncology and inflammatory disease programs. Suitable for solid-phase and solution-phase peptide-like synthesis due to the protected piperidi

Used in pharmaceutical research as an intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell proliferation. Its structure supports the development of compounds with high selectivity and binding affinity to specific enzyme sites. Commonly utilized in medicinal chemistry for optimizing drug candidates in oncology and inflammatory disease programs. Suitable for solid-phase and solution-phase peptide-like synthesis due to the protected piperidine and carboxylic acid functionalities.

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