(S)-tert-Butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate

≥95%

Reagent Code: #60151
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CAS Number 274692-08-9

science Other reagents with same CAS 274692-08-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD12828827
thermostat Physical Properties
Boiling Point 297.5±13.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring an aminoethyl group and a protected pyrrolidine ring, makes it valuable for constructing complex drug candidates, particularly in the field of central nervous system (CNS) therapeutics. It is often employed in the preparation of compounds targeting receptors or enzymes involved in neurological disorders. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing specificity and reducing potential side effects. The tert-butyloxycarbonyl (Boc) protecting group in its structure facilitates selective reactions during multi-step synthetic processes, making it a versatile building block in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿5,139.00
inventory 100mg
10-20 days ฿12,861.00

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(S)-tert-Butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate
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This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring an aminoethyl group and a protected pyrrolidine ring, makes it valuable for constructing complex drug candidates, particularly in the field of central nervous system (CNS) therapeutics. It is often employed in the preparation of compounds targeting receptors or enzymes involved in neurological disorders. Additionally, its chiral n

This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring an aminoethyl group and a protected pyrrolidine ring, makes it valuable for constructing complex drug candidates, particularly in the field of central nervous system (CNS) therapeutics. It is often employed in the preparation of compounds targeting receptors or enzymes involved in neurological disorders. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing specificity and reducing potential side effects. The tert-butyloxycarbonyl (Boc) protecting group in its structure facilitates selective reactions during multi-step synthetic processes, making it a versatile building block in medicinal chemistry.

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