2-(Benzyloxy)-5-chloropyridine

97%

Reagent Code: #153110
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CAS Number 215437-47-1

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blur_circular Chemical Specifications

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Weight 219.67 g/mol
Formula C₁₂H₁₀ClNO
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological and psychiatric disorders. It plays a key role in constructing pyridine-based scaffolds found in bioactive molecules. Commonly employed in the preparation of selective receptor modulators, including those acting on serotonin and dopamine pathways. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity in cross-coupling reactions. Its benzyl-protected hydroxyl group allows for selective deprotection and further functionalization in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,920.00
inventory 250mg
10-20 days ฿8,380.00
inventory 1g
10-20 days ฿24,630.00

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2-(Benzyloxy)-5-chloropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological and psychiatric disorders. It plays a key role in constructing pyridine-based scaffolds found in bioactive molecules. Commonly employed in the preparation of selective receptor modulators, including those acting on serotonin and dopamine pathways. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity in cross-coupli

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological and psychiatric disorders. It plays a key role in constructing pyridine-based scaffolds found in bioactive molecules. Commonly employed in the preparation of selective receptor modulators, including those acting on serotonin and dopamine pathways. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity in cross-coupling reactions. Its benzyl-protected hydroxyl group allows for selective deprotection and further functionalization in multi-step organic syntheses.

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