Methyl 3-chloro-5-methylpyrazine-2-carboxylate

≥95%

Reagent Code: #208888
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CAS Number 859063-65-3

science Other reagents with same CAS 859063-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.60 g/mol
Formula C₇H₇ClN₂O₂
badge Registry Numbers
MDL Number MFCD10697746
thermostat Physical Properties
Boiling Point 265.6±35.0°C at 760 mmHg
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 antihypertensive and antiviral agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building pyrazine-based drug candidates. Commonly employed in coupling reactions and nucleophilic substitutions to introduce the pyrazine ring into larger bioactive molecules. Also utilized in agrochemical research for designing novel pesticides due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,020.00
inventory 250mg
10-20 days ฿7,500.00
inventory 1g
10-20 days ฿29,930.00

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Methyl 3-chloro-5-methylpyrazine-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antihypertensive and antiviral agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building pyrazine-based drug candidates. Commonly employed in coupling reactions and nucleophilic substitutions to introduce the pyrazine ring into larger bioactive molecules. Also utilized in agrochemical research for designing novel pesticides due to its stability and

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antihypertensive and antiviral agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building pyrazine-based drug candidates. Commonly employed in coupling reactions and nucleophilic substitutions to introduce the pyrazine ring into larger bioactive molecules. Also utilized in agrochemical research for designing novel pesticides due to its stability and reactivity profile.

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