1-(4-Cyanophenyl)piperidine-4-carbohydrazide

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Reagent Code: #167031
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CAS Number 352018-91-8

science Other reagents with same CAS 352018-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.29 g/mol
Formula C₁₃H₁₆N₄O
badge Registry Numbers
MDL Number MFCD03086202
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of bioactive molecules. Its hydrazide functional group enables the formation of Schiff bases, which are often explored for their antimicrobial, anti-inflammatory, and anticancer properties. The presence of a nitrile group enhances its utility in constructing heterocyclic compounds, making it valuable in the design of novel drug candidates. It is also employed in the synthesis of piperidine-based derivatives that show potential in central nervous system-related therapeutic applications due to their structural similarity to neuroactive agents.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿18,180.00
inventory 250mg
10-20 days ฿9,090.00

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1-(4-Cyanophenyl)piperidine-4-carbohydrazide
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Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of bioactive molecules. Its hydrazide functional group enables the formation of Schiff bases, which are often explored for their antimicrobial, anti-inflammatory, and anticancer properties. The presence of a nitrile group enhances its utility in constructing heterocyclic compounds, making it valuable in the design of novel drug candidates. It is also employed in the synthesis of pip
Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of bioactive molecules. Its hydrazide functional group enables the formation of Schiff bases, which are often explored for their antimicrobial, anti-inflammatory, and anticancer properties. The presence of a nitrile group enhances its utility in constructing heterocyclic compounds, making it valuable in the design of novel drug candidates. It is also employed in the synthesis of piperidine-based derivatives that show potential in central nervous system-related therapeutic applications due to their structural similarity to neuroactive agents.
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