(R)-2-(Aminoethyl)-1-N-Boc-pyrrolidine

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Reagent Code: #231148
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CAS Number 550378-07-9

science Other reagents with same CAS 550378-07-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD04115290
thermostat Physical Properties
Boiling Point 297.5 °C at 760 mmHg
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 active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other biologically active compounds where stereochemistry plays a critical role in activity. Also utilized in the production of specialty intermediates for drug discovery research, especially in central nervous system (CNS) agents and antiviral drugs. The Boc-protected group ensures stability during reactions and can be easily deprotected under mild acidic conditions, making it ideal for solid-phase and solution-phase peptide-like synthesis.

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inventory 1g
10-20 days ฿7,800.00
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(R)-2-(Aminoethyl)-1-N-Boc-pyrrolidine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other biologically active compounds where stereochemistry plays a critical role in activity. Also utilized in the production of specialty intermediates for drug discovery res

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other biologically active compounds where stereochemistry plays a critical role in activity. Also utilized in the production of specialty intermediates for drug discovery research, especially in central nervous system (CNS) agents and antiviral drugs. The Boc-protected group ensures stability during reactions and can be easily deprotected under mild acidic conditions, making it ideal for solid-phase and solution-phase peptide-like synthesis.

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