5-(1-Hydroxyethyl)-2-methylpyridine

97%

Reagent Code: #194785
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CAS Number 100189-16-0

science Other reagents with same CAS 100189-16-0

blur_circular Chemical Specifications

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Weight 137.18 g/mol
Formula C₈H₁₁NO
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acid derivatives and vitamin B3 (niacin) analogs. It serves as a building block in medicinal chemistry for developing drugs targeting neurological and metabolic disorders. Also employed in the preparation of chiral catalysts and ligands for asymmetric synthesis, contributing to the development of enantioselective reactions in drug manufacturing. Its hydroxyl and methyl functional groups allow for easy modification, making it valuable in creating diverse compound libraries for drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,810.00
inventory 1g
10-20 days ฿5,230.00

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5-(1-Hydroxyethyl)-2-methylpyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acid derivatives and vitamin B3 (niacin) analogs. It serves as a building block in medicinal chemistry for developing drugs targeting neurological and metabolic disorders. Also employed in the preparation of chiral catalysts and ligands for asymmetric synthesis, contributing to the development of enantioselective reactions in drug manufacturing. Its hydroxyl and methyl functional groups allow for easy

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acid derivatives and vitamin B3 (niacin) analogs. It serves as a building block in medicinal chemistry for developing drugs targeting neurological and metabolic disorders. Also employed in the preparation of chiral catalysts and ligands for asymmetric synthesis, contributing to the development of enantioselective reactions in drug manufacturing. Its hydroxyl and methyl functional groups allow for easy modification, making it valuable in creating diverse compound libraries for drug discovery.

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