(3S,4S)-tert-Butyl 3-amino-4-fluoropyrrolidine-1-carboxylate

95%

Reagent Code: #236082
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CAS Number 1009075-43-7

science Other reagents with same CAS 1009075-43-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.24 g/mol
Formula C₉H₁₇FN₂O₂
badge Registry Numbers
MDL Number MFCD11111576
thermostat Physical Properties
Boiling Point 266°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antidiabetic agents. Its structure supports the formation of peptidomimetics and enzyme inhibitors due to the presence of a fluorinated pyrrolidine core with defined stereochemistry. Commonly employed in medicinal chemistry for constructing bioactive molecules where metabolic stability and target selectivity are critical. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection during multi-step syntheses, making it valuable in solid-phase and solution-phase peptide-like drug development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,150.00
inventory 250mg
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿17,600.00
inventory 5g
10-20 days ฿56,000.00
(3S,4S)-tert-Butyl 3-amino-4-fluoropyrrolidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antidiabetic agents. Its structure supports the formation of peptidomimetics and enzyme inhibitors due to the presence of a fluorinated pyrrolidine core with defined stereochemistry. Commonly employed in medicinal chemistry for constructing bioactive molecules where metabolic stability and target selectivity are critical. The tert-butyl carbamate (Boc) group allows for easy protection a

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antidiabetic agents. Its structure supports the formation of peptidomimetics and enzyme inhibitors due to the presence of a fluorinated pyrrolidine core with defined stereochemistry. Commonly employed in medicinal chemistry for constructing bioactive molecules where metabolic stability and target selectivity are critical. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection during multi-step syntheses, making it valuable in solid-phase and solution-phase peptide-like drug development.

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