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

≥95%

Reagent Code: #173543
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CAS Number 345311-03-7

science Other reagents with same CAS 345311-03-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.27 g/mol
Formula C₁₁H₁₇N₃O₂
badge Registry Numbers
MDL Number MFCD09878590
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. Its structure allows for selective functionalization, making it valuable in the development of kinase inhibitors and CNS-targeted drugs. Commonly employed in medicinal chemistry for building heterocyclic scaffolds due to its stability and reactivity profile. Also utilized in solid-phase and solution-phase peptide-like synthesis where protection of the nitrogen is required for controlled coupling reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿950.00
inventory 1g
10-20 days ฿3,530.00
inventory 5g
10-20 days ฿13,900.00
inventory 10g
10-20 days ฿24,160.00

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7-Boc-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure allows for selective functionalization, making it valuable in the development of kinase inhibitors and CNS-targeted drugs. Commonly employed in medicinal chemistry for building heterocyclic scaffolds due to its stability and reactivity profile. Also utilized in solid-phase and solution-phase peptide-like synthesis where protection of the nitrogen is required for controlled

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure allows for selective functionalization, making it valuable in the development of kinase inhibitors and CNS-targeted drugs. Commonly employed in medicinal chemistry for building heterocyclic scaffolds due to its stability and reactivity profile. Also utilized in solid-phase and solution-phase peptide-like synthesis where protection of the nitrogen is required for controlled coupling reactions.

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