tert-Butyl6-((tert-Butoxycarbonyl)amino)-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate
≥95%
Reagent
Code: #57057
CAS Number
959246-52-7
blur_circular Chemical Specifications
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Molecular Information
Weight
363.41 g/mol
Formula
C₁₈H₂₅N₃O₅
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Registry Numbers
MDL Number
MFCD09878781
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Physical Properties
Boiling Point
476.9 °C at 760 mmHg
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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.
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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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