1-Boc-2-pyrrolidinemethanol

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Reagent Code: #143474
label
Alias 2-hydroxymethylpyrrolidine-1-carboxylic acid butyl ester N-(tert-butoxycarbonyl)-DL-proline 1-Boc-2-pyrrolidine methanol N-Boc-DL-proline 1-(tert-butoxycarbonyl)-2-pyrrolidine methanol
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CAS Number 170491-63-1

science Other reagents with same CAS 170491-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.27 g/mol
Formula C₁₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD01456556
thermostat Physical Properties
Boiling Point 290℃
inventory_2 Storage & Handling
Density 1.084
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require chiral pyrrolidine scaffolds. Its protected amine and unprotected alcohol functionalities allow selective reactions during multi-step syntheses. Commonly employed in the production of nootropic drugs and antiviral agents. Also utilized in research settings for building complex heterocyclic compounds due to its structural versatility and stability under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿500.00
inventory 25g
10-20 days ฿2,350.00

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1-Boc-2-pyrrolidinemethanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require chiral pyrrolidine scaffolds. Its protected amine and unprotected alcohol functionalities allow selective reactions during multi-step syntheses. Commonly employed in the production of nootropic drugs and antiviral agents. Also utilized in research settings for building complex heterocyclic compounds due to its structural versatility and stability under v

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require chiral pyrrolidine scaffolds. Its protected amine and unprotected alcohol functionalities allow selective reactions during multi-step syntheses. Commonly employed in the production of nootropic drugs and antiviral agents. Also utilized in research settings for building complex heterocyclic compounds due to its structural versatility and stability under various reaction conditions.

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