(R)-2-(pyrrolidin-2-yl)pyridine

95%

Reagent Code: #230876
fingerprint
CAS Number 130464-05-0

science Other reagents with same CAS 130464-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 148.20 g/mol
Formula C₉H₁₂N₂
badge Registry Numbers
MDL Number MFCD07374401
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor ligands. It serves as an intermediate in the production of nootropic and neuroprotective agents. Its structural similarity to nicotine allows exploration in treatments for neurological disorders such as Alzheimer's and Parkinson's diseases. Also employed in asymmetric synthesis due to its stereochemical stability and ability to direct enantioselective reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,500.00
inventory 250mg
10-20 days ฿35,000.00
inventory 1g
10-20 days ฿70,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-2-(pyrrolidin-2-yl)pyridine
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor ligands. It serves as an intermediate in the production of nootropic and neuroprotective agents. Its structural similarity to nicotine allows exploration in treatments for neurological disorders such as Alzheimer's and Parkinson's diseases. Also employed in asymmetric synthesis due to its stereochemical stability and ability to direct enantioselective reactions.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor ligands. It serves as an intermediate in the production of nootropic and neuroprotective agents. Its structural similarity to nicotine allows exploration in treatments for neurological disorders such as Alzheimer's and Parkinson's diseases. Also employed in asymmetric synthesis due to its stereochemical stability and ability to direct enantioselective reactions.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...