2-(2-Methylpiperidin-1-yl)ethanol

95%

Reagent Code: #211882
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CAS Number 17719-74-3

science Other reagents with same CAS 17719-74-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.23 g/mol
Formula C₈H₁₇NO
badge Registry Numbers
MDL Number MFCD11613834
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of central nervous system agents and analgesics. It serves as a building block for active pharmaceutical ingredients due to its structural compatibility with bioactive molecules. Commonly employed in the development of local anesthetics and antipsychotic drugs, where the piperidine ring contributes to receptor binding affinity. Also utilized in the preparation of agrochemicals and specialty chemicals requiring chiral amine functionalities. Its hydroxyl group allows for easy modification, enabling conjugation or attachment to larger molecular frameworks in drug design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,960.00
inventory 1g
10-20 days ฿9,700.00

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2-(2-Methylpiperidin-1-yl)ethanol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of central nervous system agents and analgesics. It serves as a building block for active pharmaceutical ingredients due to its structural compatibility with bioactive molecules. Commonly employed in the development of local anesthetics and antipsychotic drugs, where the piperidine ring contributes to receptor binding affinity. Also utilized in the preparation of agrochemicals and specialty chemicals requiring chi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of central nervous system agents and analgesics. It serves as a building block for active pharmaceutical ingredients due to its structural compatibility with bioactive molecules. Commonly employed in the development of local anesthetics and antipsychotic drugs, where the piperidine ring contributes to receptor binding affinity. Also utilized in the preparation of agrochemicals and specialty chemicals requiring chiral amine functionalities. Its hydroxyl group allows for easy modification, enabling conjugation or attachment to larger molecular frameworks in drug design.

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