2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine hydrochloride

98%

Reagent Code: #158592
label
Alias 2-Chloromethyl-3,5 dimethyl-4-methoxypyridine hydrochloride; 3,5-dimethyl-2-chloromethyl-4-methoxypyridine hydrochloride
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CAS Number 86604-75-3

science Other reagents with same CAS 86604-75-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.11 g/mol
Formula C₉H₁₂ClNO·HCl
badge Registry Numbers
MDL Number MFCD00277472
thermostat Physical Properties
Melting Point 128-131 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as an intermediate in the synthesis of proton pump inhibitors (PPIs), particularly omeprazole and related drugs. It plays a key role in forming the pyridine core structure required for the biological activity of these anti-ulcer medications. The chloromethyl group allows for further alkylation or coupling reactions, enabling the attachment of benzimidazole moieties in the final drug molecule. Widely utilized in pharmaceutical manufacturing due to its reactivity and stability in controlled conditions.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿150.00
inventory 100g
10-20 days ฿910.00
inventory 500g
10-20 days ฿4,310.00
inventory 25g
10-20 days ฿310.00

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2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine hydrochloride
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Used as an intermediate in the synthesis of proton pump inhibitors (PPIs), particularly omeprazole and related drugs. It plays a key role in forming the pyridine core structure required for the biological activity of these anti-ulcer medications. The chloromethyl group allows for further alkylation or coupling reactions, enabling the attachment of benzimidazole moieties in the final drug molecule. Widely utilized in pharmaceutical manufacturing due to its reactivity and stability in controlled conditions

Used as an intermediate in the synthesis of proton pump inhibitors (PPIs), particularly omeprazole and related drugs. It plays a key role in forming the pyridine core structure required for the biological activity of these anti-ulcer medications. The chloromethyl group allows for further alkylation or coupling reactions, enabling the attachment of benzimidazole moieties in the final drug molecule. Widely utilized in pharmaceutical manufacturing due to its reactivity and stability in controlled conditions.

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