(R)-1-(5-Methylfuran-2-yl)propan-1-aMine

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Reagent Code: #37351
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CAS Number 473732-94-4

science Other reagents with same CAS 473732-94-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.19 g/mol
Formula C₈H₁₃NO
inventory_2 Storage & Handling
Storage 2-8℃, avoid light

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical research industries as a chiral building block for the synthesis of more complex molecules. Its structure, featuring a furan ring and an amine group, makes it valuable in the development of enantioselective drugs and bioactive compounds. It is often employed in asymmetric synthesis to create intermediates for potential therapeutic agents, particularly in the design of compounds targeting the central nervous system. Additionally, its unique stereochemistry allows for its use in the study of enzyme interactions and receptor binding, aiding in the discovery of new drug candidates.

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inventory 1g
10-20 days ฿52,020.00

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(R)-1-(5-Methylfuran-2-yl)propan-1-aMine
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This compound is primarily utilized in the pharmaceutical and chemical research industries as a chiral building block for the synthesis of more complex molecules. Its structure, featuring a furan ring and an amine group, makes it valuable in the development of enantioselective drugs and bioactive compounds. It is often employed in asymmetric synthesis to create intermediates for potential therapeutic agents, particularly in the design of compounds targeting the central nervous system. Additionally, its u

This compound is primarily utilized in the pharmaceutical and chemical research industries as a chiral building block for the synthesis of more complex molecules. Its structure, featuring a furan ring and an amine group, makes it valuable in the development of enantioselective drugs and bioactive compounds. It is often employed in asymmetric synthesis to create intermediates for potential therapeutic agents, particularly in the design of compounds targeting the central nervous system. Additionally, its unique stereochemistry allows for its use in the study of enzyme interactions and receptor binding, aiding in the discovery of new drug candidates.

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