Tert-butyl2-methyl-5,8-dihydropyrido[3,4-d]pyrimidine-7(6H)-carboxylate

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Reagent Code: #244359
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CAS Number 1346808-81-8

science Other reagents with same CAS 1346808-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.31 g/mol
Formula C₁₃H₁₉N₃O₂
badge Registry Numbers
MDL Number MFCD19688629
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in optimizing drug potency and metabolic stability during medicinal chemistry research. Commonly employed in late-stage functionalization due to the protective role of the tert-butyl carbamate (Boc) group, which facilitates controlled deprotection and further coupling reactions in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,730.00
inventory 250mg
10-20 days ฿6,360.00
inventory 1g
10-20 days ฿17,360.00

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Tert-butyl2-methyl-5,8-dihydropyrido[3,4-d]pyrimidine-7(6H)-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in optimizing drug potency and metabolic stability during medicinal chemistry research. Commonly employed in late-stage functionalization due to the protective role of the tert-butyl carbamate (Boc) group, which facilitates controlled deprotection and further coupling reactions in multi-step syn

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in optimizing drug potency and metabolic stability during medicinal chemistry research. Commonly employed in late-stage functionalization due to the protective role of the tert-butyl carbamate (Boc) group, which facilitates controlled deprotection and further coupling reactions in multi-step synthetic routes.

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