Ethyl 3-bromo-6-cyclopropylpicolinate

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Reagent Code: #45319
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CAS Number 908833-44-3

science Other reagents with same CAS 908833-44-3

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Weight 270.1225 g/mol
Formula C₁₁H₁₂BrNO₂
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the synthesis of agrochemicals and pharmaceuticals, where its structure serves as a building block for active ingredients. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse chemical entities. Additionally, its cyclopropyl group can impart unique steric and electronic properties to the final compounds, making it useful in the design of molecules with specific biological activities. Researchers also employ this compound in the study of structure-activity relationships to optimize the efficacy of potential drug candidates.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,163.00

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Ethyl 3-bromo-6-cyclopropylpicolinate
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This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the synthesis of agrochemicals and pharmaceuticals, where its structure serves as a building block for active ingredients. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse chemical entities. Additionally,

This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the synthesis of agrochemicals and pharmaceuticals, where its structure serves as a building block for active ingredients. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse chemical entities. Additionally, its cyclopropyl group can impart unique steric and electronic properties to the final compounds, making it useful in the design of molecules with specific biological activities. Researchers also employ this compound in the study of structure-activity relationships to optimize the efficacy of potential drug candidates.

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