3-amino-1-methylpiperidine-2,6-dionehydrochloride

98%

Reagent Code: #139376
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CAS Number 1909304-98-8

science Other reagents with same CAS 1909304-98-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.62 g/mol
Formula C₆H₁₁ClN₂O₂
badge Registry Numbers
MDL Number MFCD28895640
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It plays a role in the production of certain anticonvulsant and neuroprotective drugs due to its structural similarity to known bioactive piperidine derivatives. Its derivatives are explored for potential use in treating neurological disorders such as epilepsy and neuropathic pain. Also utilized in research settings for structure-activity relationship studies in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,750.00
inventory 250mg
10-20 days ฿17,070.00
inventory 1g
10-20 days ฿46,540.00

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3-amino-1-methylpiperidine-2,6-dionehydrochloride
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It plays a role in the production of certain anticonvulsant and neuroprotective drugs due to its structural similarity to known bioactive piperidine derivatives. Its derivatives are explored for potential use in treating neurological disorders such as epilepsy and neuropathic pain. Also utilized in research settings for structure-activity relationship studies in medicina

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It plays a role in the production of certain anticonvulsant and neuroprotective drugs due to its structural similarity to known bioactive piperidine derivatives. Its derivatives are explored for potential use in treating neurological disorders such as epilepsy and neuropathic pain. Also utilized in research settings for structure-activity relationship studies in medicinal chemistry.

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