(S)-2-Amino-2-(naphthalen-1-yl)ethan-1-ol

≥97%

Reagent Code: #38243
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CAS Number 110480-82-5

science Other reagents with same CAS 110480-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₁₂H₁₃NO
badge Registry Numbers
MDL Number MFCD09253738
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its structure, featuring a naphthalene ring and an amino alcohol moiety, makes it valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds. It is also employed in the preparation of ligands for catalysis, enhancing the efficiency of chemical reactions in organic synthesis. Additionally, it finds use in research settings for studying enzyme inhibition and receptor binding due to its unique stereochemical properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,820.00

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(S)-2-Amino-2-(naphthalen-1-yl)ethan-1-ol
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This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its structure, featuring a naphthalene ring and an amino alcohol moiety, makes it valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds. It is also employed in the preparation of ligands for catalysis, enhancing the efficiency of chemical reactions in organic synthesis. Additionally, it

This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its structure, featuring a naphthalene ring and an amino alcohol moiety, makes it valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds. It is also employed in the preparation of ligands for catalysis, enhancing the efficiency of chemical reactions in organic synthesis. Additionally, it finds use in research settings for studying enzyme inhibition and receptor binding due to its unique stereochemical properties.

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