Methyl 5-chloro-6-methoxynicotinate

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Reagent Code: #207354
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CAS Number 220656-93-9

science Other reagents with same CAS 220656-93-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.61 g/mol
Formula C₈H₈ClNO₃
badge Registry Numbers
MDL Number MFCD12025914
thermostat Physical Properties
Melting Point 108-110°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 nicotinic receptor modulators and central nervous system agents. Its structure supports the creation of bioactive molecules with potential applications in treating neurological disorders. Also employed in agrochemical research for designing novel pesticides due to its ability to enhance binding selectivity in target enzymes. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,480.00
inventory 250mg
10-20 days ฿1,970.00
inventory 1g
10-20 days ฿2,420.00

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Methyl 5-chloro-6-methoxynicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and central nervous system agents. Its structure supports the creation of bioactive molecules with potential applications in treating neurological disorders. Also employed in agrochemical research for designing novel pesticides due to its ability to enhance binding selectivity in target enzymes. Commonly utilized in medicinal chemistry for scaffold modification and structure-ac

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and central nervous system agents. Its structure supports the creation of bioactive molecules with potential applications in treating neurological disorders. Also employed in agrochemical research for designing novel pesticides due to its ability to enhance binding selectivity in target enzymes. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship studies.

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