tert-Butyl 2-(hydroxymethyl)-5,6-dihydroimidazo[1,2-a]pyrazine-7(8H)-carboxylate
≥95%
Reagent
Code: #115951
CAS Number
1250996-70-3
blur_circular Chemical Specifications
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Molecular Information
Weight
253.30 g/mol
Formula
C₁₂H₁₉N₃O₃
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Registry Numbers
MDL Number
MFCD18792756
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Physical Properties
Boiling Point
462.9°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, dry and sealed
description Product Description
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. It plays a significant role in the development of heterocyclic molecules, which are often explored for their potential therapeutic applications. Specifically, it is used in the construction of imidazo[1,2-a]pyrazine derivatives, a class of compounds known for their pharmacological properties, including anti-inflammatory, antiviral, and anticancer activities. Its structure allows for further functionalization, making it a versatile building block in drug discovery and development processes. Additionally, it is employed in research laboratories to study structure-activity relationships (SAR) and optimize drug candidates for enhanced efficacy and selectivity.
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tert-Butyl 2-(hydroxymethyl)-5,6-dihydroimidazo[1,2-a]pyrazine-7(8H)-carboxylate
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. It plays a significant role in the development of heterocyclic molecules, which are often explored for their potential therapeutic applications. Specifically, it is used in the construction of imidazo[1,2-a]pyrazine derivatives, a class of compounds known for their pharmacological properties, including anti-inflammatory, antiviral, and anticancer activities. Its structure allows for further functionalization, making it a versatile building block in drug discovery and development processes. Additionally, it is employed in research laboratories to study structure-activity relationships (SAR) and optimize drug candidates for enhanced efficacy and selectivity.
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