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

98%

Reagent Code: #146482
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CAS Number 1105187-42-5

science Other reagents with same CAS 1105187-42-5

blur_circular Chemical Specifications

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Weight 236.27 g/mol
Formula C₁₁H₁₆N₄O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of pharmaceuticals targeting cancer and inflammatory diseases. Its protected amine group allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in solid-phase and solution-phase peptide-like synthesis where stability and selective deprotection are required. Also utilized in the preparation of nucleoside analogs and as a scaffold in drug discovery for optimizing potency and metabolic stability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿720.00
inventory 5g
10-20 days ฿8,450.00
inventory 1g
10-20 days ฿2,340.00

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tert-Butyl 2-amino-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate
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Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of pharmaceuticals targeting cancer and inflammatory diseases. Its protected amine group allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in solid-phase and solution-phase peptide-like synthesis where stability and selective deprotection are required. Also utilized in the preparation of nucleoside analogs and as a s

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of pharmaceuticals targeting cancer and inflammatory diseases. Its protected amine group allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in solid-phase and solution-phase peptide-like synthesis where stability and selective deprotection are required. Also utilized in the preparation of nucleoside analogs and as a scaffold in drug discovery for optimizing potency and metabolic stability.

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