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

≥95%

Reagent Code: #235708
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CAS Number 287966-92-1

science Other reagents with same CAS 287966-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.13 g/mol
Formula C₉H₁₄Cl₂N₂
badge Registry Numbers
MDL Number MFCD28369439
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used 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 modulators, which are investigated for treating neurological disorders such as Alzheimer's disease, schizophrenia, and depression. Its structural configuration supports high receptor selectivity, making it valuable in optimizing drug efficacy and reducing side effects. Also employed in asymmetric synthesis due to its stereochemical stability and ability to direct enantioselective transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,300.00
inventory 250mg
10-20 days ฿3,130.00

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(S)-3-(Pyrrolidin-2-yl)pyridine dihydrochloride
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Used 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 modulators, which are investigated for treating neurological disorders such as Alzheimer's disease, schizophrenia, and depression. Its structural configuration supports high receptor selectivity, making it valuable in optimizing drug efficacy and reducing side effects. Also employed in asymmetric synthesis due to its ste

Used 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 modulators, which are investigated for treating neurological disorders such as Alzheimer's disease, schizophrenia, and depression. Its structural configuration supports high receptor selectivity, making it valuable in optimizing drug efficacy and reducing side effects. Also employed in asymmetric synthesis due to its stereochemical stability and ability to direct enantioselective transformations.

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