6-phenyl-1-(trideuteriomethyl)imidazo[4,5-b]pyridin-2-amine

AR

Reagent Code: #91801
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CAS Number 210049-13-1

science Other reagents with same CAS 210049-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.2797 g/mol
Formula C₁₃H₉D₃N₄
thermostat Physical Properties
Melting Point >300°C
inventory_2 Storage & Handling
Density 1.318g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzyme pathways or receptors. Its structure is often incorporated into drug candidates designed for therapeutic applications, such as anti-inflammatory, antiviral, or anticancer agents. Additionally, the deuterium substitution in the molecule enhances its metabolic stability, making it valuable in the development of deuterated drugs, which can exhibit improved pharmacokinetic properties. Researchers also use it in isotope labeling studies to track metabolic pathways and understand drug behavior in biological systems.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿38,080.00

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6-phenyl-1-(trideuteriomethyl)imidazo[4,5-b]pyridin-2-amine
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzyme pathways or receptors. Its structure is often incorporated into drug candidates designed for therapeutic applications, such as anti-inflammatory, antiviral, or anticancer agents. Additionally, the deuterium substitution in the molecule enhances its metabolic stability, ma

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzyme pathways or receptors. Its structure is often incorporated into drug candidates designed for therapeutic applications, such as anti-inflammatory, antiviral, or anticancer agents. Additionally, the deuterium substitution in the molecule enhances its metabolic stability, making it valuable in the development of deuterated drugs, which can exhibit improved pharmacokinetic properties. Researchers also use it in isotope labeling studies to track metabolic pathways and understand drug behavior in biological systems.

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