(R)-3-Benzyl-N,N',N'-trimethylpiperidine-3-carbohydrazide dihydrochloride

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Reagent Code: #232273
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CAS Number 883572-50-7

science Other reagents with same CAS 883572-50-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.31 g/mol
Formula C₁₆H₂₇Cl₂N₃O
badge Registry Numbers
MDL Number MFCD29472302
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used in pharmaceutical research as a chiral intermediate for the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its hydrazide functionality allows for derivatization into heterocyclic structures, which are common scaffolds in drug design. The compound's stereochemistry makes it valuable in asymmetric synthesis, where the (R)-enantiomer can influence the potency and selectivity of resulting molecules. It has also been explored in the preparation of enzyme inhibitors, especially those targeting proteases and amidases. Due to its amine and hydrazide groups, it serves as a building block in combinatorial chemistry for generating compound libraries aimed at identifying new therapeutic candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿37,980.00
inventory 250mg
10-20 days ฿64,550.00

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(R)-3-Benzyl-N,N',N'-trimethylpiperidine-3-carbohydrazide dihydrochloride
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Used in pharmaceutical research as a chiral intermediate for the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its hydrazide functionality allows for derivatization into heterocyclic structures, which are common scaffolds in drug design. The compound's stereochemistry makes it valuable in asymmetric synthesis, where the (R)-enantiomer can influence the potency and selectivity of resulting molecules. It has also been explored in the preparati

Used in pharmaceutical research as a chiral intermediate for the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its hydrazide functionality allows for derivatization into heterocyclic structures, which are common scaffolds in drug design. The compound's stereochemistry makes it valuable in asymmetric synthesis, where the (R)-enantiomer can influence the potency and selectivity of resulting molecules. It has also been explored in the preparation of enzyme inhibitors, especially those targeting proteases and amidases. Due to its amine and hydrazide groups, it serves as a building block in combinatorial chemistry for generating compound libraries aimed at identifying new therapeutic candidates.

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