Ethyl 2-(3-bromopyridin-2-yl)acetate

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Reagent Code: #182403
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CAS Number 197376-41-3

science Other reagents with same CAS 197376-41-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD10566269
thermostat Physical Properties
Boiling Point 278°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. 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 50mg
10-20 days ฿300.00
inventory 250mg
10-20 days ฿960.00
inventory 1g
10-20 days ฿3,390.00
inventory 5g
10-20 days ฿14,180.00

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Ethyl 2-(3-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 bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. 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 no

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. 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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