tert-Butyl 5-bromonicotinate

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Reagent Code: #49097
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CAS Number 263270-02-6

science Other reagents with same CAS 263270-02-6

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scatter_plot Molecular Information
Weight 258.1118 g/mol
Formula C₁₀H₁₂BrNO₂
badge Registry Numbers
MDL Number MFCD07367903
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description Product Description

This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring a bromine atom and an ester group, makes it suitable for various coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential in creating biologically active compounds. Additionally, it is utilized in agrochemical research for the synthesis of novel pesticides or herbicides. Its versatility in chemical transformations makes it a key reagent in the development of diverse chemical products.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿650.00
inventory 250mg
10-20 days ฿980.00
inventory 1g
10-20 days ฿2,300.00
inventory 25g
10-20 days ฿29,210.00
inventory 5g
10-20 days ฿7,570.00

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tert-Butyl 5-bromonicotinate
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This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring a bromine atom and an ester group, makes it suitable for various coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential in creating biologically active compounds. Additionally,

This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring a bromine atom and an ester group, makes it suitable for various coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential in creating biologically active compounds. Additionally, it is utilized in agrochemical research for the synthesis of novel pesticides or herbicides. Its versatility in chemical transformations makes it a key reagent in the development of diverse chemical products.

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