tert-Butyl 2-(hydroxymethyl)-5,6-dihydroimidazo[1,2-a]pyrazine-7(8H)-carboxylate

≥95%

Reagent Code: #115951
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CAS Number 1250996-70-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.30 g/mol
Formula C₁₂H₁₉N₃O₃
badge Registry Numbers
MDL Number MFCD18792756
thermostat Physical Properties
Boiling Point 462.9°C at 760 mmHg
inventory_2 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days $195.72
inventory 250mg
10-20 days $392.21
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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