Methyl 2-(5-bromopyridin-2-yl)acetate

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Reagent Code: #208997
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CAS Number 917023-06-4

science Other reagents with same CAS 917023-06-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.06 g/mol
Formula C₈H₈BrNO₂
badge Registry Numbers
MDL Number MFCD12031821
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon bonds in drug discovery pathways. Also utilized in agrochemical research for designing novel active ingredients.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,360.00
inventory 5g
10-20 days ฿5,440.00
inventory 10g
10-20 days ฿10,790.00
inventory 25g
10-20 days ฿26,950.00

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Methyl 2-(5-bromopyridin-2-yl)acetate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon bonds in drug discovery pathways. Also utilized in agrochemical research for designing novel

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon bonds in drug discovery pathways. Also utilized in agrochemical research for designing novel active ingredients.

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