3R)-oxolan-3-ylmethanamine hydrochloride

97%

Reagent Code: #232327
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CAS Number 1400744-17-3

science Other reagents with same CAS 1400744-17-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.61 g/mol
Formula C₅H₁₂ClNO
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MDL Number MFCD20526349
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 amine functionality allows for coupling reactions in peptide-like structures or heterocyclic systems. Commonly employed in the preparation of neuroactive compounds and enzyme inhibitors due to its structural similarity to proline derivatives. Also utilized in asymmetric synthesis where the (R)-configuration plays a critical role in biological activity or catalytic processes. Stable as a hydrochloride salt, making it suitable for storage and handling in industrial-scale reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿50,880.00
3R)-oxolan-3-ylmethanamine hydrochloride
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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 amine functionality allows for coupling reactions in peptide-like structures or heterocyclic systems. Commonly employed in the preparation of neuroactive compounds and enzyme inhibitors due to its structural similarity to proline derivatives. Also utilized in asymmetric synthesis where the (R)-configuration plays a critica

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 amine functionality allows for coupling reactions in peptide-like structures or heterocyclic systems. Commonly employed in the preparation of neuroactive compounds and enzyme inhibitors due to its structural similarity to proline derivatives. Also utilized in asymmetric synthesis where the (R)-configuration plays a critical role in biological activity or catalytic processes. Stable as a hydrochloride salt, making it suitable for storage and handling in industrial-scale reactions.

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