Methyl 3-bromo-6-chloropyrazine-2-carboxylate

95%

Reagent Code: #210363
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CAS Number 13457-28-8

science Other reagents with same CAS 13457-28-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.47 g/mol
Formula C₆H₄BrClN₂O₂
badge Registry Numbers
MDL Number MFCD13195362
thermostat Physical Properties
Melting Point 258-259 °C
Boiling Point 433.7±55.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antibacterial agents. Its functional groups allow for selective modifications, making it valuable in constructing complex heterocyclic compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive halogen atoms that facilitate coupling reactions. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,310.00
inventory 1g
10-20 days ฿5,100.00
inventory 5g
10-20 days ฿17,930.00
Methyl 3-bromo-6-chloropyrazine-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antibacterial agents. Its functional groups allow for selective modifications, making it valuable in constructing complex heterocyclic compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive halogen atoms that facilitate coupling reactions. 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 antiviral and antibacterial agents. Its functional groups allow for selective modifications, making it valuable in constructing complex heterocyclic compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive halogen atoms that facilitate coupling reactions. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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