2-(Chloromethyl)-4-methoxy-3-methylpyridine hydrochloride

98%

Reagent Code: #165200
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CAS Number 86604-74-2

science Other reagents with same CAS 86604-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.09 g/mol
Formula C₈H₁₁Cl₂NO
badge Registry Numbers
MDL Number MFCD03425333
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of proton pump inhibitors such as omeprazole and esomeprazole, which are widely prescribed for treating gastric acid-related disorders including gastroesophageal reflux disease (GERD) and peptic ulcers. Its structure allows for efficient coupling reactions in the formation of benzimidazole derivatives, making it valuable in pharmaceutical manufacturing. The hydrochloride salt form enhances stability and solubility during synthesis steps. Commonly employed in multi-step organic transformations under controlled conditions to ensure high yield and purity of the final active pharmaceutical ingredients.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿740.00
inventory 25g
10-20 days ฿2,470.00
inventory 100g
10-20 days ฿7,600.00
inventory 500g
10-20 days ฿23,000.00

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2-(Chloromethyl)-4-methoxy-3-methylpyridine hydrochloride
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Used as an intermediate in the synthesis of proton pump inhibitors such as omeprazole and esomeprazole, which are widely prescribed for treating gastric acid-related disorders including gastroesophageal reflux disease (GERD) and peptic ulcers. Its structure allows for efficient coupling reactions in the formation of benzimidazole derivatives, making it valuable in pharmaceutical manufacturing. The hydrochloride salt form enhances stability and solubility during synthesis steps. Commonly employed in multi

Used as an intermediate in the synthesis of proton pump inhibitors such as omeprazole and esomeprazole, which are widely prescribed for treating gastric acid-related disorders including gastroesophageal reflux disease (GERD) and peptic ulcers. Its structure allows for efficient coupling reactions in the formation of benzimidazole derivatives, making it valuable in pharmaceutical manufacturing. The hydrochloride salt form enhances stability and solubility during synthesis steps. Commonly employed in multi-step organic transformations under controlled conditions to ensure high yield and purity of the final active pharmaceutical ingredients.

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