4-(3-nitrophenyl)-1,2,3,6-tetrahydropyridinehydrochloride

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Reagent Code: #220565
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CAS Number 2409597-54-0

science Other reagents with same CAS 2409597-54-0

blur_circular Chemical Specifications

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Weight 240.69 g/mol
Formula C₁₁H₁₃ClN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Particularly valuable in the development of nitrogen-containing heterocyclic systems. Commonly employed in the preparation of substituted pyridines and piperidines, which are structural motifs in various medicinal agents. Also utilized in research settings for the synthesis of potential neuroactive agents and receptor ligands. Its nitro-substituted aryl group allows for further functionalization through reduction or coupling reactions, making it a versatile building block in drug discovery and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,090.00

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4-(3-nitrophenyl)-1,2,3,6-tetrahydropyridinehydrochloride
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Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Particularly valuable in the development of nitrogen-containing heterocyclic systems. Commonly employed in the preparation of substituted pyridines and piperidines, which are structural motifs in various medicinal agents. Also utilized in research settings for the synthesis of potential neuroactive agents and receptor ligands. Its nitro-substituted aryl group allows for further functionalization through re

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Particularly valuable in the development of nitrogen-containing heterocyclic systems. Commonly employed in the preparation of substituted pyridines and piperidines, which are structural motifs in various medicinal agents. Also utilized in research settings for the synthesis of potential neuroactive agents and receptor ligands. Its nitro-substituted aryl group allows for further functionalization through reduction or coupling reactions, making it a versatile building block in drug discovery and materials science.

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