2-(Hydroxymethyl)piperidine
98%
Reagent
Code: #85156
Alias
2-Hydroxymethylpiperidine
CAS Number
3433-37-2
blur_circular Chemical Specifications
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Molecular Information
Weight
115.18 g/mol
Formula
C₆H₁₃NO
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Registry Numbers
MDL Number
MFCD00005987
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Storage & Handling
Storage
room temperature, sealed
description Product Description
2-(Hydroxymethyl)piperidine is widely used in organic synthesis as a versatile building block for the preparation of various pharmaceuticals and bioactive compounds. Its structure, featuring both a hydroxyl group and a piperidine ring, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. It is also employed as a chiral auxiliary or ligand in asymmetric synthesis, aiding in the creation of enantiomerically pure compounds. Additionally, it serves as an intermediate in the production of agrochemicals, such as herbicides and fungicides, due to its ability to modify biological activity. In material science, it is utilized in the synthesis of polymers and coatings, where its functional groups contribute to enhanced properties like adhesion and durability.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Melting Point | 68-70 |
Purity | 98-100% |
Appearance | Yellow powder |
Infrared Spectrometry | Conforms to Structure |
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2-(Hydroxymethyl)piperidine
2-(Hydroxymethyl)piperidine is widely used in organic synthesis as a versatile building block for the preparation of various pharmaceuticals and bioactive compounds. Its structure, featuring both a hydroxyl group and a piperidine ring, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. It is also employed as a chiral auxiliary or ligand in asymmetric synthesis, aiding in the creation of enantiomerically pure compounds. Additionally, it serves as an intermediate in the production of agrochemicals, such as herbicides and fungicides, due to its ability to modify biological activity. In material science, it is utilized in the synthesis of polymers and coatings, where its functional groups contribute to enhanced properties like adhesion and durability.
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