tert-Butyl 4-chloro-5,6-dihydropyrido[4',3':4,5]thieno[2,3-d]pyrimidine-7(8H)-carboxylate

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Reagent Code: #150270
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CAS Number 946198-89-6

science Other reagents with same CAS 946198-89-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.81 g/mol
Formula C₁₄H₁₆ClN₃O₂S
badge Registry Numbers
MDL Number MFCD09754437
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents targeting kinase inhibition, particularly in oncology research. Its structure supports the development of small molecule inhibitors that modulate signaling pathways in cancer cells. Commonly employed in medicinal chemistry for constructing dihydropyridopyrimidine-based scaffolds with potential antitumor activity. Also utilized in structure-activity relationship (SAR) studies to optimize potency and selectivity of drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,140.00
inventory 1g
10-20 days ฿5,760.00
inventory 5g
10-20 days ฿18,970.00

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tert-Butyl 4-chloro-5,6-dihydropyrido[4',3':4,5]thieno[2,3-d]pyrimidine-7(8H)-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents targeting kinase inhibition, particularly in oncology research. Its structure supports the development of small molecule inhibitors that modulate signaling pathways in cancer cells. Commonly employed in medicinal chemistry for constructing dihydropyridopyrimidine-based scaffolds with potential antitumor activity. Also utilized in structure-activity relationship (SAR) studies to optimize potency and selectivity of drug candidates.

Used as a key intermediate in the synthesis of pharmaceutical agents targeting kinase inhibition, particularly in oncology research. Its structure supports the development of small molecule inhibitors that modulate signaling pathways in cancer cells. Commonly employed in medicinal chemistry for constructing dihydropyridopyrimidine-based scaffolds with potential antitumor activity. Also utilized in structure-activity relationship (SAR) studies to optimize potency and selectivity of drug candidates.

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