tert-Butyl 3-iodo-2-methyl-6,7-dihydropyrazolo[1,5-a]pyrazine-5(4H)-carboxylate

95%

Reagent Code: #83696
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CAS Number 2138122-16-2

science Other reagents with same CAS 2138122-16-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.1935 g/mol
Formula C₁₂H₁₈IN₃O₂
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Widely utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the development of novel drug candidates, targeting various therapeutic areas including central nervous system disorders and oncology. The presence of the iodo group at position 3 allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for screening purposes. Additionally, the tert-butyl ester moiety provides protection for the carboxyl group during multi-step synthetic processes, ensuring selective reactivity at other sites. This compound's versatility makes it an essential building block in medicinal chemistry, particularly in the design of heterocyclic compounds with potential therapeutic applications. Its stability and reactivity profile also make it suitable for use in automated synthesis platforms, facilitating high-throughput drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿7,200.00
inventory 100mg
10-20 days ฿21,600.00

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tert-Butyl 3-iodo-2-methyl-6,7-dihydropyrazolo[1,5-a]pyrazine-5(4H)-carboxylate
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Widely utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the development of novel drug candidates, targeting various therapeutic areas including central nervous system disorders and oncology. The presence of the iodo group at position 3 allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for screening purposes. Ad

Widely utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the development of novel drug candidates, targeting various therapeutic areas including central nervous system disorders and oncology. The presence of the iodo group at position 3 allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for screening purposes. Additionally, the tert-butyl ester moiety provides protection for the carboxyl group during multi-step synthetic processes, ensuring selective reactivity at other sites. This compound's versatility makes it an essential building block in medicinal chemistry, particularly in the design of heterocyclic compounds with potential therapeutic applications. Its stability and reactivity profile also make it suitable for use in automated synthesis platforms, facilitating high-throughput drug discovery efforts.

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