(S)-1-(6-Bromopyridin-2-yl)ethanamine

95%

Reagent Code: #37936
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CAS Number 323584-38-9

science Other reagents with same CAS 323584-38-9

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Weight 201.0638 g/mol
Formula C₇H₉BrN₂
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Storage room temperature

description Product Description

This compound is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a bromopyridine moiety and a chiral center, makes it a valuable building block for developing pharmaceuticals, particularly in the design of ligands for receptor targeting. It is often employed in the creation of compounds with potential applications in treating neurological disorders, as the pyridine ring can interact with specific enzymes or receptors in the brain. Additionally, its (S)-chirality allows for the development of enantioselective drugs, enhancing therapeutic efficacy and reducing side effects. Researchers also utilize it in the study of structure-activity relationships to optimize drug candidates for improved potency and selectivity.

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inventory 100mg
10-20 days ฿15,066.00

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(S)-1-(6-Bromopyridin-2-yl)ethanamine
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This compound is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a bromopyridine moiety and a chiral center, makes it a valuable building block for developing pharmaceuticals, particularly in the design of ligands for receptor targeting. It is often employed in the creation of compounds with potential applications in treating neurological disorders, as the pyridine ring can interact with specific enzymes

This compound is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a bromopyridine moiety and a chiral center, makes it a valuable building block for developing pharmaceuticals, particularly in the design of ligands for receptor targeting. It is often employed in the creation of compounds with potential applications in treating neurological disorders, as the pyridine ring can interact with specific enzymes or receptors in the brain. Additionally, its (S)-chirality allows for the development of enantioselective drugs, enhancing therapeutic efficacy and reducing side effects. Researchers also utilize it in the study of structure-activity relationships to optimize drug candidates for improved potency and selectivity.

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