1-Boc-3-ethynyl-3-hydroxypyrrolidine

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Reagent Code: #140896
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CAS Number 275387-76-3

science Other reagents with same CAS 275387-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.258 g/mol
Formula C₁₁H₁₇NO₃
badge Registry Numbers
MDL Number MFCD23106002
thermostat Physical Properties
Boiling Point 292.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in pharmaceutical synthesis as a protected intermediate for constructing bioactive molecules, particularly in the development of protease inhibitors and central nervous system agents. The Boc-protected hydroxyl-ethynyl pyrrolidine scaffold allows for selective functionalization via click chemistry or cross-coupling reactions, enabling efficient assembly of complex heterocyclic compounds. Its structural features support conformational control and hydrogen bonding, making it valuable in medicinal chemistry for optimizing potency and metabolic stability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,400.00

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1-Boc-3-ethynyl-3-hydroxypyrrolidine
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Used in pharmaceutical synthesis as a protected intermediate for constructing bioactive molecules, particularly in the development of protease inhibitors and central nervous system agents. The Boc-protected hydroxyl-ethynyl pyrrolidine scaffold allows for selective functionalization via click chemistry or cross-coupling reactions, enabling efficient assembly of complex heterocyclic compounds. Its structural features support conformational control and hydrogen bonding, making it valuable in medicinal chem

Used in pharmaceutical synthesis as a protected intermediate for constructing bioactive molecules, particularly in the development of protease inhibitors and central nervous system agents. The Boc-protected hydroxyl-ethynyl pyrrolidine scaffold allows for selective functionalization via click chemistry or cross-coupling reactions, enabling efficient assembly of complex heterocyclic compounds. Its structural features support conformational control and hydrogen bonding, making it valuable in medicinal chemistry for optimizing potency and metabolic stability.

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