Ethyl 4,5-dibromo-1H-imidazole-2-carboxylate

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Reagent Code: #182837
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CAS Number 74840-99-6

science Other reagents with same CAS 74840-99-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.93 g/mol
Formula C₆H₆Br₂N₂O₂
badge Registry Numbers
MDL Number MFCD21496615
thermostat Physical Properties
Melting Point 154-156°C
Boiling Point 389.6±45.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and anticancer compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings to prepare imidazole-based derivatives that exhibit biological activity. Also utilized in the design of kinase inhibitors and other enzyme-targeted therapies. Its bromine substituents enable cross-coupling reactions, facilitating the introduction of diverse molecular fragments in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,380.00
inventory 250mg
10-20 days ฿3,280.00
inventory 1g
10-20 days ฿12,550.00
inventory 5g
10-20 days ฿46,400.00
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Ethyl 4,5-dibromo-1H-imidazole-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and anticancer compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings to prepare imidazole-based derivatives that exhibit biological activity. Also utilized in the design of kinase inhibitors and other enzyme-targeted therapies. Its bromine substituents enable

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and anticancer compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings to prepare imidazole-based derivatives that exhibit biological activity. Also utilized in the design of kinase inhibitors and other enzyme-targeted therapies. Its bromine substituents enable cross-coupling reactions, facilitating the introduction of diverse molecular fragments in drug discovery programs.

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