Methyl 2H-indazole-7-carboxylate

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Reagent Code: #208910
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CAS Number 952479-65-1

science Other reagents with same CAS 952479-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.17 g/mol
Formula C₉H₈N₂O₂
badge Registry Numbers
MDL Number MFCD22683960
thermostat Physical Properties
Boiling Point 232.7±23.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used primarily in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of cannabinoid receptor modulators. Its structure serves as a core scaffold in creating analogs for studying neurological pathways and potential therapeutics for pain management, inflammation, and neurodegenerative diseases. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its favorable binding properties and metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿850.00
inventory 250mg
10-20 days ฿2,120.00
inventory 1g
10-20 days ฿8,050.00

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Methyl 2H-indazole-7-carboxylate
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Used primarily in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of cannabinoid receptor modulators. Its structure serves as a core scaffold in creating analogs for studying neurological pathways and potential therapeutics for pain management, inflammation, and neurodegenerative diseases. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its favorable binding properties and metabolic stabil

Used primarily in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of cannabinoid receptor modulators. Its structure serves as a core scaffold in creating analogs for studying neurological pathways and potential therapeutics for pain management, inflammation, and neurodegenerative diseases. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its favorable binding properties and metabolic stability.

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