[(2R)-Oxolan-2-yl]methanamine hydrochloride

95%

Reagent Code: #231472
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CAS Number 7175-80-6

science Other reagents with same CAS 7175-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.61 g/mol
Formula C₅H₁₂ClNO
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MDL Number MFCD00192476
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its cyclic amine structure makes it valuable for creating enantiomerically pure compounds, especially in the production of drugs targeting central nervous system disorders and cardiovascular diseases. Commonly employed in asymmetric synthesis and catalysis due to its ability to direct stereoselective transformations. Also utilized in the preparation of intermediates for protease inhibitors and other biologically active molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,320.00
inventory 1g
10-20 days ฿6,240.00
inventory 5g
10-20 days ฿29,120.00
[(2R)-Oxolan-2-yl]methanamine 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) where stereochemistry plays a critical role. Its cyclic amine structure makes it valuable for creating enantiomerically pure compounds, especially in the production of drugs targeting central nervous system disorders and cardiovascular diseases. Commonly employed in asymmetric synthesis and catalysis due to its ability to direct stereoselective transformations.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its cyclic amine structure makes it valuable for creating enantiomerically pure compounds, especially in the production of drugs targeting central nervous system disorders and cardiovascular diseases. Commonly employed in asymmetric synthesis and catalysis due to its ability to direct stereoselective transformations. Also utilized in the preparation of intermediates for protease inhibitors and other biologically active molecules.

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