tert-Butyl6-((tert-Butoxycarbonyl)amino)-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate

≥95%

Reagent Code: #57057
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CAS Number 959246-52-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.41 g/mol
Formula C₁₈H₂₅N₃O₅
badge Registry Numbers
MDL Number MFCD09878781
thermostat Physical Properties
Boiling Point 476.9 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic applications. The presence of the tert-butoxycarbonyl (Boc) protecting group makes it valuable in peptide synthesis, where it safeguards amino groups during reactions. Additionally, its structure is useful in the creation of quinoxaline derivatives, which are explored for their biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Its role in facilitating controlled and selective reactions makes it a critical component in medicinal chemistry and drug discovery processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,150.00
inventory 250mg
10-20 days ฿5,580.00
tert-Butyl6-((tert-Butoxycarbonyl)amino)-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate
This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic applications. The presence of the tert-butoxycarbonyl (Boc) protecting group makes it valuable in peptide synthesis, where it safeguards amino groups during reactions. Additionally, its structure is useful in the creation of quinoxaline derivatives, which are explored for their biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Its role in facilitating controlled and selective reactions makes it a critical component in medicinal chemistry and drug discovery processes.
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