tert-Butyl N-[(1S)-2-(methanesulfonyloxy)-1-phenylethyl]carbamate

95%

Reagent Code: #82863
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CAS Number 110143-62-9

science Other reagents with same CAS 110143-62-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.39 g/mol
Formula C₁₄H₂₁NO₅S
badge Registry Numbers
MDL Number MFCD22420311
thermostat Physical Properties
Melting Point 113-115 °C
Boiling Point 497.2±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.204±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It plays a key role in the synthesis of chiral compounds, often serving as a protected form of an amine group during multi-step reactions. The methanesulfonyloxy group in the structure makes it a useful precursor for nucleophilic substitution reactions, enabling the introduction of various functional groups. Its application is significant in the development of enantiomerically pure drugs, where the chiral center is crucial for biological activity. Additionally, it is employed in peptide chemistry for the protection of amino acids, ensuring selective reactivity in peptide bond formation.

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Test Parameter Specification
Appearance Light yellow powder
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,300.00
inventory 250mg
10-20 days ฿10,800.00
inventory 1g
10-20 days ฿21,294.00

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tert-Butyl N-[(1S)-2-(methanesulfonyloxy)-1-phenylethyl]carbamate
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This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It plays a key role in the synthesis of chiral compounds, often serving as a protected form of an amine group during multi-step reactions. The methanesulfonyloxy group in the structure makes it a useful precursor for nucleophilic substitution reactions, enabling the introduction of various functional groups. Its application is significant in t

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It plays a key role in the synthesis of chiral compounds, often serving as a protected form of an amine group during multi-step reactions. The methanesulfonyloxy group in the structure makes it a useful precursor for nucleophilic substitution reactions, enabling the introduction of various functional groups. Its application is significant in the development of enantiomerically pure drugs, where the chiral center is crucial for biological activity. Additionally, it is employed in peptide chemistry for the protection of amino acids, ensuring selective reactivity in peptide bond formation.

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