[(2S)-1,4-dioxan-2-yl]methyl(methyl)amine hydrochloride

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Reagent Code: #37857
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CAS Number 2055848-87-6

science Other reagents with same CAS 2055848-87-6

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Weight 167.6339 g/mol
Formula C₆H₁₄ClNO₂
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MDL Number MFCD30530563
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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 various pharmaceuticals. Its structure, featuring a dioxane ring and an amine group, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting the central nervous system. Additionally, it is employed in the synthesis of ligands for catalysts, aiding in asymmetric synthesis processes. Its hydrochloride form enhances solubility, making it easier to handle and incorporate into reaction mixtures. The compound’s versatility also extends to its use in research for studying receptor interactions and enzyme inhibition, contributing to the discovery of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,478.00

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[(2S)-1,4-dioxan-2-yl]methyl(methyl)amine hydrochloride
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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 various pharmaceuticals. Its structure, featuring a dioxane ring and an amine group, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting the central nervous system. Additionally, it is employed in the synthesis of ligands for catalysts, aiding in asymmetric synthesis processes. Its hydrochloride form enhances solubility, mak

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring a dioxane ring and an amine group, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting the central nervous system. Additionally, it is employed in the synthesis of ligands for catalysts, aiding in asymmetric synthesis processes. Its hydrochloride form enhances solubility, making it easier to handle and incorporate into reaction mixtures. The compound’s versatility also extends to its use in research for studying receptor interactions and enzyme inhibition, contributing to the discovery of new therapeutic agents.

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