Methyl 2-bromo-1H-imidazole-5-carboxylate

95%

Reagent Code: #202936
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CAS Number 1379311-82-6

science Other reagents with same CAS 1379311-82-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.01 g/mol
Formula C₅H₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD18633459
thermostat Physical Properties
Boiling Point 341.8±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.781±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure, featuring a bromo group at the 2-position and a methyl carboxylate at the 5-position, allows for selective modifications such as cross-coupling reactions, making it valuable in creating biologically active molecules. Commonly employed in medicinal chemistry for constructing imidazole-based drug candidates. Also utilized in agrochemical research for designing new active ingredients in crop protection products.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,580.00
inventory 250mg
10-20 days ฿18,840.00
inventory 1g
10-20 days ฿53,040.00
Methyl 2-bromo-1H-imidazole-5-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure, featuring a bromo group at the 2-position and a methyl carboxylate at the 5-position, allows for selective modifications such as cross-coupling reactions, making it valuable in creating biologically active molecules. Commonly employed in medicinal chemistry for constructing imidazole-based drug candidates. Also utilized in agrochemical research for designing n

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure, featuring a bromo group at the 2-position and a methyl carboxylate at the 5-position, allows for selective modifications such as cross-coupling reactions, making it valuable in creating biologically active molecules. Commonly employed in medicinal chemistry for constructing imidazole-based drug candidates. Also utilized in agrochemical research for designing new active ingredients in crop protection products.

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