3-Chloro-4-hydroxymethyl-2-methoxypyridine

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Reagent Code: #163751
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CAS Number 1227586-24-4

science Other reagents with same CAS 1227586-24-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.60 g/mol
Formula C₇H₈ClNO₂
badge Registry Numbers
MDL Number MFCD16607033
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of proton pump inhibitors like omeprazole and related drugs. Its structure allows for selective functionalization, making it valuable in constructing active pharmaceutical ingredients that target gastric acid secretion. Commonly employed in multi-step organic syntheses where the chloro and hydroxymethyl groups serve as reactive sites for further modification. Also utilized in the development of agrochemicals due to its pyridine backbone, which is prevalent in bioactive molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,770.00
inventory 1g
10-20 days ฿5,060.00
inventory 5g
10-20 days ฿21,840.00

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3-Chloro-4-hydroxymethyl-2-methoxypyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of proton pump inhibitors like omeprazole and related drugs. Its structure allows for selective functionalization, making it valuable in constructing active pharmaceutical ingredients that target gastric acid secretion. Commonly employed in multi-step organic syntheses where the chloro and hydroxymethyl groups serve as reactive sites for further modification. Also utilized in the development of agrochemicals due t

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of proton pump inhibitors like omeprazole and related drugs. Its structure allows for selective functionalization, making it valuable in constructing active pharmaceutical ingredients that target gastric acid secretion. Commonly employed in multi-step organic syntheses where the chloro and hydroxymethyl groups serve as reactive sites for further modification. Also utilized in the development of agrochemicals due to its pyridine backbone, which is prevalent in bioactive molecules.

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