(R)-3-(Pyrrolidin-2-yl)pyridine dihydrochloride

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Reagent Code: #230519
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CAS Number 288247-82-5

science Other reagents with same CAS 288247-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.13 g/mol
Formula C₉H₁₄Cl₂N₂
badge Registry Numbers
MDL Number MFCD30478933
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used primarily in pharmaceutical research as a chiral building block for the synthesis of neuroactive compounds. It serves as an intermediate in the development of nicotinic acetylcholine receptor (nAChR) modulators, which are investigated for treating neurological disorders such as depression, cognitive impairment, and neuropathic pain. Its structural configuration allows selective interaction with receptor subtypes, making it valuable in structure-activity relationship (SAR) studies. Also employed in the preparation of radiolabeled derivatives for use in receptor binding assays and positron emission tomography (PET) imaging probes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,660.00
inventory 250mg
10-20 days ฿16,590.00

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(R)-3-(Pyrrolidin-2-yl)pyridine dihydrochloride
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Used primarily in pharmaceutical research as a chiral building block for the synthesis of neuroactive compounds. It serves as an intermediate in the development of nicotinic acetylcholine receptor (nAChR) modulators, which are investigated for treating neurological disorders such as depression, cognitive impairment, and neuropathic pain. Its structural configuration allows selective interaction with receptor subtypes, making it valuable in structure-activity relationship (SAR) studies. Also employed in t

Used primarily in pharmaceutical research as a chiral building block for the synthesis of neuroactive compounds. It serves as an intermediate in the development of nicotinic acetylcholine receptor (nAChR) modulators, which are investigated for treating neurological disorders such as depression, cognitive impairment, and neuropathic pain. Its structural configuration allows selective interaction with receptor subtypes, making it valuable in structure-activity relationship (SAR) studies. Also employed in the preparation of radiolabeled derivatives for use in receptor binding assays and positron emission tomography (PET) imaging probes.

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