3-([2,2'-Bipyridin]-5-yl)-2-aminopropanoic acid hydrochloride

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Reagent Code: #44452
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CAS Number 2044702-29-4

science Other reagents with same CAS 2044702-29-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.72 g/mol
Formula C₁₃H₁₄ClN₃O₂
badge Registry Numbers
MDL Number MFCD30543760
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This compound is primarily utilized in the field of chemical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the creation of ligands for coordination chemistry, which are essential in the study of metal complexes and catalysis. Its bipyridyl moiety makes it valuable in the design of materials for photochemical applications, such as solar cells and light-emitting devices, due to its ability to facilitate electron transfer processes. Additionally, it is employed in the preparation of bioactive compounds, including potential pharmaceuticals, where its structural features contribute to binding affinity and specificity in biological systems. Its hydrochloride form enhances solubility, making it more convenient for use in aqueous reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,227.00
inventory 250mg
10-20 days ฿27,063.00
inventory 25mg
10-20 days ฿6,633.00

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3-([2,2'-Bipyridin]-5-yl)-2-aminopropanoic acid hydrochloride
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This compound is primarily utilized in the field of chemical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the creation of ligands for coordination chemistry, which are essential in the study of metal complexes and catalysis. Its bipyridyl moiety makes it valuable in the design of materials for photochemical applications, such as solar cells and light-emitting devices, due to its ability to facilitate electron transfer processes. Additionally, it is employed in the preparation of bioactive compounds, including potential pharmaceuticals, where its structural features contribute to binding affinity and specificity in biological systems. Its hydrochloride form enhances solubility, making it more convenient for use in aqueous reaction conditions.
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