methyl 2-((benzylamino)methyl)-3-hydroxybutanoate

Reagent Code: #50403
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CAS Number 118558-99-9

science Other reagents with same CAS 118558-99-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.29 g/mol
Formula C₁₃H₁₉NO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both hydroxyl and ester functional groups, makes it versatile for various chemical reactions, including esterification and amidation processes. In pharmaceutical research, it is often employed in the development of potential drug candidates, particularly those targeting neurological disorders, due to its ability to interact with specific biological pathways. Additionally, it is used in the synthesis of chiral compounds, which are crucial in the manufacture of enantiomerically pure substances for medicinal and industrial applications. Its benzylamino group also allows for further modifications, enabling the creation of diverse chemical libraries for screening purposes.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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methyl 2-((benzylamino)methyl)-3-hydroxybutanoate
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both hydroxyl and ester functional groups, makes it versatile for various chemical reactions, including esterification and amidation processes. In pharmaceutical research, it is often employed in the development of potential drug candidates, particularly those targeting neurological disorders, due to its ability to interact with

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both hydroxyl and ester functional groups, makes it versatile for various chemical reactions, including esterification and amidation processes. In pharmaceutical research, it is often employed in the development of potential drug candidates, particularly those targeting neurological disorders, due to its ability to interact with specific biological pathways. Additionally, it is used in the synthesis of chiral compounds, which are crucial in the manufacture of enantiomerically pure substances for medicinal and industrial applications. Its benzylamino group also allows for further modifications, enabling the creation of diverse chemical libraries for screening purposes.

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