(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

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Reagent Code: #37819
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CAS Number 170097-58-2

science Other reagents with same CAS 170097-58-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.30 g/mol
Formula C₁₁H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD31729566
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of peptides and other biologically active molecules. It is particularly valuable in the protection of amine groups during multi-step synthetic processes, ensuring selective reactions and preventing unwanted side reactions. Its structure allows for efficient deprotection under mild conditions, making it suitable for constructing complex molecular frameworks. Additionally, it finds application in the development of pharmaceuticals, especially in the synthesis of chiral compounds where stereochemical integrity is crucial. Its role in facilitating the production of enantiomerically pure substances is significant in drug discovery and development.

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Test Parameter Specification
Appearance Colorless to pale yellow liquid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,669.00
inventory 100mg
10-20 days ฿3,330.00

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(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)(methyl)carbamate
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This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of peptides and other biologically active molecules. It is particularly valuable in the protection of amine groups during multi-step synthetic processes, ensuring selective reactions and preventing unwanted side reactions. Its structure allows for efficient deprotection under mild conditions, making it suitable for constructing complex molecular frameworks. Additionally, it finds application in the development of pharmaceuticals, especially in the synthesis of chiral compounds where stereochemical integrity is crucial. Its role in facilitating the production of enantiomerically pure substances is significant in drug discovery and development.
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