5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester

98%

Reagent Code: #151284
label
Alias 5-bromo-3-methylpyridine-2-carboxylic acid methyl ester; 5-bromo-3-methylpyridine-2-carboxylic acid methyl ester; methyl 5-bromo-3-methylpyridine-2-carboxylic acid methyl ester
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CAS Number 213771-32-5

science Other reagents with same CAS 213771-32-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.05862 g/mol
Formula C₈H₈BrNO₂
badge Registry Numbers
MDL Number MFCD07375126
thermostat Physical Properties
Boiling Point 302.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, 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 selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing new crop protection agents due to its stability and reactivity profile.

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Test Parameter Specification
Appearance White to yellow solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿162.00
inventory 1g
10-20 days ฿500.00
inventory 5g
10-20 days ฿1,218.00
inventory 25g
10-20 days ฿5,298.00
inventory 100g
10-20 days ฿33,680.00

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5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester
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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 selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing new crop protection agents d

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 selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing new crop protection agents due to its stability and reactivity profile.

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