(2R,4S)-2-Hydroxymethyl-4-Boc-aminopyrrolidine hydrochloride

≥95%

Reagent Code: #112984
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CAS Number 1865786-36-2

science Other reagents with same CAS 1865786-36-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.74 g/mol
Formula C₁₀H₂₁ClN₂O₃
badge Registry Numbers
MDL Number MFCD11042662
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of various therapeutic agents, including antiviral and anticancer drugs. Its chiral structure makes it valuable in creating enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in peptide synthesis, where it acts as a building block for constructing complex peptide chains. Its Boc-protected amino group allows for selective deprotection, enabling precise control over chemical reactions in multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,017.00
inventory 250mg
10-20 days ฿15,426.00
inventory 1g
10-20 days ฿47,403.00

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(2R,4S)-2-Hydroxymethyl-4-Boc-aminopyrrolidine hydrochloride
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of various therapeutic agents, including antiviral and anticancer drugs. Its chiral structure makes it valuable in creating enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in peptide synthesis, where it acts as a building block
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of various therapeutic agents, including antiviral and anticancer drugs. Its chiral structure makes it valuable in creating enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in peptide synthesis, where it acts as a building block for constructing complex peptide chains. Its Boc-protected amino group allows for selective deprotection, enabling precise control over chemical reactions in multi-step synthetic processes.
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