2-Bromo-3-methylisonicotinonitrile

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Reagent Code: #80858
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CAS Number 1260024-26-7

science Other reagents with same CAS 1260024-26-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.03 g/mol
Formula C₇H₅BrN₂
badge Registry Numbers
MDL Number MFCD28665862
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring both a bromine atom and a nitrile group, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the methyl-substituted pyridine moiety into target molecules. Additionally, it is used in the development of agrochemicals and biologically active compounds, particularly those targeting specific enzymes or receptors. Its reactivity also makes it valuable in the synthesis of heterocyclic compounds, which are crucial in medicinal chemistry for drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,228.00
inventory 250mg
10-20 days ฿10,575.00
inventory 1g
10-20 days ฿28,548.00

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2-Bromo-3-methylisonicotinonitrile
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring both a bromine atom and a nitrile group, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the methyl-substituted pyridine moiety into target molecules. Additionally, it is used in the

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring both a bromine atom and a nitrile group, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the methyl-substituted pyridine moiety into target molecules. Additionally, it is used in the development of agrochemicals and biologically active compounds, particularly those targeting specific enzymes or receptors. Its reactivity also makes it valuable in the synthesis of heterocyclic compounds, which are crucial in medicinal chemistry for drug discovery and development.

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