Methyl 5-bromo-2-methylnicotinate

98%

Reagent Code: #210161
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CAS Number 1215916-40-7

science Other reagents with same CAS 1215916-40-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.06 g/mol
Formula C₈H₈BrNO₂
badge Registry Numbers
MDL Number MFCD13705366
thermostat Physical Properties
Boiling Point 245.2±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and kinase inhibitors. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems due to the presence of reactive bromo and ester functional groups. Facilitates cross-coupling reactions such as Suzuki or Heck reactions, enabling the introduction of aryl or alkenyl moieties. Also utilized in agrochemical research for designing novel pesticides with improved biological activity. Its methyl ester group can be hydrolyzed to yield carboxylic acid derivatives for further functionalization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿860.00
inventory 1g
10-20 days ฿2,940.00
inventory 5g
10-20 days ฿14,460.00
inventory 25g
10-20 days ฿42,490.00

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Methyl 5-bromo-2-methylnicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and kinase inhibitors. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems due to the presence of reactive bromo and ester functional groups. Facilitates cross-coupling reactions such as Suzuki or Heck reactions, enabling the introduction of aryl or alkenyl moieties. Also utilized in agrochemical research for designing novel pesticides with im

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and kinase inhibitors. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems due to the presence of reactive bromo and ester functional groups. Facilitates cross-coupling reactions such as Suzuki or Heck reactions, enabling the introduction of aryl or alkenyl moieties. Also utilized in agrochemical research for designing novel pesticides with improved biological activity. Its methyl ester group can be hydrolyzed to yield carboxylic acid derivatives for further functionalization.

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