(S)-2-(Bromomethyl)-1-methylpyrrolidine

97%

Reagent Code: #234898
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CAS Number 60365-88-0

science Other reagents with same CAS 60365-88-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.07 g/mol
Formula C₆H₁₂BrN
thermostat Physical Properties
Boiling Point 179.0±13.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for central nervous system drugs. Its bromomethyl group enables alkylation reactions, making it valuable for constructing complex organic molecules. Commonly employed in the development of nicotinic receptor agonists and cognitive enhancers. Also utilized in asymmetric synthesis due to its stereochemical purity, supporting the creation of enantiomerically pure compounds in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,500.00
inventory 100mg
10-20 days ฿6,030.00
(S)-2-(Bromomethyl)-1-methylpyrrolidine
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for central nervous system drugs. Its bromomethyl group enables alkylation reactions, making it valuable for constructing complex organic molecules. Commonly employed in the development of nicotinic receptor agonists and cognitive enhancers. Also utilized in asymmetric synthesis due to its stereochemical purity, supporting the creation of enantiomerically pure compounds in medicinal

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for central nervous system drugs. Its bromomethyl group enables alkylation reactions, making it valuable for constructing complex organic molecules. Commonly employed in the development of nicotinic receptor agonists and cognitive enhancers. Also utilized in asymmetric synthesis due to its stereochemical purity, supporting the creation of enantiomerically pure compounds in medicinal chemistry research.

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