(Z)-N-(1-(2-Bromophenyl)-1-chloro-3-oxo-3-(piperidin-1-yl)prop-1-en-2-yl)benzamide

≥95%

Reagent Code: #113875
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CAS Number 1800044-77-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 447.75 g/mol
Formula C₂₁H₂₀BrClN₂O₂
badge Registry Numbers
MDL Number MFCD29037407
thermostat Physical Properties
Boiling Point 634.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of pharmacologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its structure, featuring a bromophenyl group and a piperidine moiety, makes it a valuable precursor for designing compounds with potential therapeutic applications. Researchers often employ it in the synthesis of novel drug candidates, especially in the study of central nervous system (CNS) disorders, due to its ability to interact with specific biological targets. Additionally, its unique chemical framework allows for further functionalization, enabling the creation of diverse derivatives for biological evaluation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,918.00
inventory 100mg
10-20 days ฿4,968.00
(Z)-N-(1-(2-Bromophenyl)-1-chloro-3-oxo-3-(piperidin-1-yl)prop-1-en-2-yl)benzamide
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of pharmacologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its structure, featuring a bromophenyl group and a piperidine moiety, makes it a valuable precursor for designing compounds with potential therapeutic applications. Researchers often employ it in the synthesis of novel drug candidates, especially in the study of central nervous system (CNS) disorders, due to its ability to interact with specific biological targets. Additionally, its unique chemical framework allows for further functionalization, enabling the creation of diverse derivatives for biological evaluation.
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