Ethyl 7-aminofuro[2,3-b]pyrazine-6-carboxylate

≥95%

Reagent Code: #183547
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CAS Number 187732-95-2

science Other reagents with same CAS 187732-95-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.19 g/mol
Formula C₉H₉N₃O₃
badge Registry Numbers
MDL Number MFCD09909670
thermostat Physical Properties
Boiling Point 345.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in medicinal chemistry research to build complex heterocyclic systems for evaluating biological activity. Suitable for use in cross-coupling reactions and functional group transformations due to its reactive amino and ester groups.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,090.00
inventory 5g
10-20 days ฿14,200.00
inventory 250mg
10-20 days ฿820.00

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Ethyl 7-aminofuro[2,3-b]pyrazine-6-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in medicinal chemistry research to build complex heterocyclic systems for evaluating biological activity. Suitable for use in cross-coupling reactions and functional group transformations due to its reactive amino and ester groups.

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in medicinal chemistry research to build complex heterocyclic systems for evaluating biological activity. Suitable for use in cross-coupling reactions and functional group transformations due to its reactive amino and ester groups.

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