(R)-2-(Piperidin-3-yl)isoindoline-1,3-dione hydrochloride
≥95%
Reagent
Code: #113550
CAS Number
1381795-31-8
blur_circular Chemical Specifications
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Molecular Information
Weight
266.72 g/mol
Formula
C₁₃H₁₅ClN₂O₂
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Registry Numbers
MDL Number
MFCD09752972
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Storage & Handling
Storage
Room temperature, dry and sealed
description Product Description
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs) targeting neurological and psychiatric disorders. Its structure, featuring a piperidine ring and isoindoline-1,3-dione moiety, makes it a valuable intermediate in designing molecules that interact with central nervous system receptors. It is often explored for its potential in creating drugs for conditions such as anxiety, depression, and cognitive impairments. Additionally, its chiral nature allows for the development of enantiomerically pure compounds, enhancing specificity and reducing side effects in therapeutic applications. Researchers also investigate its use in the development of enzyme inhibitors and modulators of biological pathways relevant to neurodegenerative diseases.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White to Off-White Solid |
Purity (%) | 94.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
shopping_cart Available Sizes & Pricing
(R)-2-(Piperidin-3-yl)isoindoline-1,3-dione hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs) targeting neurological and psychiatric disorders. Its structure, featuring a piperidine ring and isoindoline-1,3-dione moiety, makes it a valuable intermediate in designing molecules that interact with central nervous system receptors. It is often explored for its potential in creating drugs for conditions such as anxiety, depression, and cognitive impairments. Additionally, its chiral nature allows for the development of enantiomerically pure compounds, enhancing specificity and reducing side effects in therapeutic applications. Researchers also investigate its use in the development of enzyme inhibitors and modulators of biological pathways relevant to neurodegenerative diseases.
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