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

98%

Reagent Code: #146382
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CAS Number 869198-95-8

science Other reagents with same CAS 869198-95-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.3 g/mol
Formula C₁₂H₁₈N₄O₂
thermostat Physical Properties
Melting Point 170-172°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure enables selective binding to enzyme targets involved in cellular signaling pathways, making it valuable in the research and production of drugs for cancer and inflammatory diseases. The tert-butyl protecting group facilitates controlled reactivity during multi-step synthesis, improving yield and purity in the preparation of active pharmaceutical ingredients.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,220.00
inventory 5g
10-20 days ฿8,870.00
inventory 25g
10-20 days ฿28,650.00

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tert-Butyl 2-amino-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure enables selective binding to enzyme targets involved in cellular signaling pathways, making it valuable in the research and production of drugs for cancer and inflammatory diseases. The tert-butyl protecting group facilitates controlled reactivity during multi-step synthesis, improving yield and purity in the preparation of active pharmaceutical ingredients.

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure enables selective binding to enzyme targets involved in cellular signaling pathways, making it valuable in the research and production of drugs for cancer and inflammatory diseases. The tert-butyl protecting group facilitates controlled reactivity during multi-step synthesis, improving yield and purity in the preparation of active pharmaceutical ingredients.

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