Ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate

95%

Reagent Code: #83641
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CAS Number 139308-52-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.06 g/mol
Formula C₇H₉BrN₂O₂
badge Registry Numbers
MDL Number MFCD22420858
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in organic synthesis as a versatile building block for the construction of more complex molecules. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring a bromo substituent and an ester group, makes it suitable for various cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in drug discovery and development. Additionally, it finds application in agrochemical research for the creation of novel compounds with potential pesticidal or herbicidal properties. Its reactivity and functional groups allow for further modifications, enabling the exploration of diverse chemical spaces in both medicinal and agricultural chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days Ft139,551.06
inventory 100mg
10-20 days Ft39,885.08
inventory 250mg
10-20 days Ft69,775.53
Ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate
This chemical is primarily used in organic synthesis as a versatile building block for the construction of more complex molecules. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring a bromo substituent and an ester group, makes it suitable for various cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in drug discovery and development. Additionally, it finds application in agrochemical research for the creation of novel compounds with potential pesticidal or herbicidal properties. Its reactivity and functional groups allow for further modifications, enabling the exploration of diverse chemical spaces in both medicinal and agricultural chemistry.
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