4-Methoxy-3,5-dimethyl-2-pyridinemethanol

98%

Reagent Code: #204764
label
Alias 4-methoxy-3,5-dimethyl-2-hydroxymethylpyridine; 4-methoxy-3,5-dimethyl-2-pyridine
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CAS Number 86604-78-6

science Other reagents with same CAS 86604-78-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.21 g/mol
Formula C₉H₁₃NO₂
badge Registry Numbers
EC Number 289-258-5
MDL Number MFCD01076195
thermostat Physical Properties
Melting Point 56.5-60.5 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of proton pump inhibitors (PPIs) like omeprazole and related derivatives. Its structure allows for selective functionalization, making it valuable in forming active pharmaceutical ingredients (APIs) that target gastric acid secretion. Commonly employed in multi-step organic synthesis due to its stability and reactivity profile. Also utilized in the development of agrochemicals and specialty heterocyclic compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿162.00
inventory 25g
10-20 days ฿350.00
inventory 100g
10-20 days ฿1,250.00
inventory 500g
10-20 days ฿5,930.00
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4-Methoxy-3,5-dimethyl-2-pyridinemethanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of proton pump inhibitors (PPIs) like omeprazole and related derivatives. Its structure allows for selective functionalization, making it valuable in forming active pharmaceutical ingredients (APIs) that target gastric acid secretion. Commonly employed in multi-step organic synthesis due to its stability and reactivity profile. Also utilized in the development of agrochemicals and specialty heterocyclic compoun

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of proton pump inhibitors (PPIs) like omeprazole and related derivatives. Its structure allows for selective functionalization, making it valuable in forming active pharmaceutical ingredients (APIs) that target gastric acid secretion. Commonly employed in multi-step organic synthesis due to its stability and reactivity profile. Also utilized in the development of agrochemicals and specialty heterocyclic compounds.

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