Ethyl 7-Boc-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine-2-carboxylate

≥97%

Reagent Code: #171865
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CAS Number 1053656-22-6

science Other reagents with same CAS 1053656-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.33 g/mol
Formula C₁₄H₂₁N₃O₄
badge Registry Numbers
MDL Number MFCD10566312
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and central nervous system agents due to its structural compatibility with heterocyclic frameworks found in drug molecules. Its protected amine group allows for selective functionalization, making it valuable in multi-step organic syntheses, especially in medicinal chemistry for optimizing lead compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,350.00
inventory 1g
10-20 days ฿4,330.00
inventory 5g
10-20 days ฿21,510.00
inventory 10g
10-20 days ฿42,960.00

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Ethyl 7-Boc-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine-2-carboxylate
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and central nervous system agents due to its structural compatibility with heterocyclic frameworks found in drug molecules. Its protected amine group allows for selective functionalization, making it valuable in multi-step organic syntheses, especially in medicinal chemistry for optimizing lead compounds.

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and central nervous system agents due to its structural compatibility with heterocyclic frameworks found in drug molecules. Its protected amine group allows for selective functionalization, making it valuable in multi-step organic syntheses, especially in medicinal chemistry for optimizing lead compounds.

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