3-(2-Pyridyl)-1-propanol Hydrochloride

≥95%

Reagent Code: #173311
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CAS Number 52225-87-3

science Other reagents with same CAS 52225-87-3

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scatter_plot Molecular Information
Weight 173.64 g/mol
Formula C₈H₁₂ClNO
badge Registry Numbers
MDL Number MFCD23381121
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting the central nervous system. It serves as a building block for pyridine-containing compounds, which are common in bioactive molecules. Its hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction conditions. Also employed in the preparation of ligands for catalytic processes and in the research of receptor agonists or antagonists due to the pyridyl group's affinity for biological targets.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,670.00
inventory 5g
10-20 days ฿8,540.00

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3-(2-Pyridyl)-1-propanol Hydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting the central nervous system. It serves as a building block for pyridine-containing compounds, which are common in bioactive molecules. Its hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction conditions. Also employed in the preparation of ligands for catalytic processes and in the research of receptor agonists or antagonists due to the pyridy

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting the central nervous system. It serves as a building block for pyridine-containing compounds, which are common in bioactive molecules. Its hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction conditions. Also employed in the preparation of ligands for catalytic processes and in the research of receptor agonists or antagonists due to the pyridyl group's affinity for biological targets.

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