S)-(1-Methylazetidin-2-yl)Methanol

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Reagent Code: #52813
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CAS Number 1310411-24-5

science Other reagents with same CAS 1310411-24-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.15 g/mol
Formula C₅H₁₁NO
thermostat Physical Properties
Boiling Point 139.2±13.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.005±0.06 g/cm3(Predicted)
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting the central nervous system. It plays a crucial role in creating molecules with potential therapeutic effects for neurological disorders. Additionally, it is utilized in organic chemistry research for the preparation of chiral building blocks, aiding in the study of stereochemistry and enantioselective reactions. Its structural properties make it valuable in designing bioactive molecules with improved efficacy and selectivity.

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inventory 1g
10-20 days ฿28,809.00

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S)-(1-Methylazetidin-2-yl)Methanol
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting the central nervous system. It plays a crucial role in creating molecules with potential therapeutic effects for neurological disorders. Additionally, it is utilized in organic chemistry research for the preparation of chiral building blocks, aiding in the study of stereochemistry and enantioselective reactions. Its structural properties make it valuable in designing bioactive molec

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting the central nervous system. It plays a crucial role in creating molecules with potential therapeutic effects for neurological disorders. Additionally, it is utilized in organic chemistry research for the preparation of chiral building blocks, aiding in the study of stereochemistry and enantioselective reactions. Its structural properties make it valuable in designing bioactive molecules with improved efficacy and selectivity.

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