Benzyl ((3aS,4R,6S,6aR)-6-(2-hydroxyethoxy)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)carbamate

97%

Reagent Code: #112985
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CAS Number 274693-54-8

science Other reagents with same CAS 274693-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.39 g/mol
Formula C₁₈H₂₅NO₆
thermostat Physical Properties
Boiling Point 524.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a protective group for amines during complex chemical reactions, ensuring the stability and specificity of the desired products. Additionally, it is employed in the preparation of modified sugars and other biologically active molecules, contributing to advancements in medicinal chemistry and drug discovery. Its role in these processes highlights its importance in creating targeted therapeutic agents.

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Test Parameter Specification
Appearance White to off-white powder or crystals
Purity (%) 96.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,720.00
inventory 250mg
10-20 days ฿2,660.00
inventory 1g
10-20 days ฿6,250.00

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Benzyl ((3aS,4R,6S,6aR)-6-(2-hydroxyethoxy)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)carbamate
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This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a protective group for amines during complex chemical reactions, ensuring the stability and specificity of the desired products. Additionally, it is employed in the preparation of modified sugars and other biologically active molecules, contributing to advancements in medicinal chemistry and drug discovery. Its role in these processes highlights its importance in creating targeted therapeutic agents.
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