Methyl 2-Amino-2-(2-pyridyl)acetate Dihydrochloride

95%

Reagent Code: #58289
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CAS Number 1039356-77-8

science Other reagents with same CAS 1039356-77-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.10 g/mol
Formula C₈H₁₂Cl₂N₂O₂
badge Registry Numbers
MDL Number MFCD22741446
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is widely utilized in organic synthesis, particularly as a building block for the preparation of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of bioactive compounds and drug candidates. Its structure, featuring both an amino group and a pyridine ring, makes it valuable for creating ligands in coordination chemistry, which are essential in catalysis and material science. Additionally, it is employed in research settings for studying biochemical pathways and designing enzyme inhibitors due to its ability to mimic natural substrates. Its dihydrochloride form enhances solubility, making it easier to handle in aqueous reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,260.00
inventory 1g
10-20 days ฿29,170.00
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Methyl 2-Amino-2-(2-pyridyl)acetate Dihydrochloride
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This compound is widely utilized in organic synthesis, particularly as a building block for the preparation of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of bioactive compounds and drug candidates. Its structure, featuring both an amino group and a pyridine ring, makes it valuable for creating ligands in coordination chemistry, which are essential in catalysis and material science. Additionally, it is employed in research settings

This compound is widely utilized in organic synthesis, particularly as a building block for the preparation of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of bioactive compounds and drug candidates. Its structure, featuring both an amino group and a pyridine ring, makes it valuable for creating ligands in coordination chemistry, which are essential in catalysis and material science. Additionally, it is employed in research settings for studying biochemical pathways and designing enzyme inhibitors due to its ability to mimic natural substrates. Its dihydrochloride form enhances solubility, making it easier to handle in aqueous reactions.

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