3-[(Dimethylamino)methyl]-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one

>95%

Reagent Code: #117589
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CAS Number 153139-56-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.35 g/mol
Formula C₁₆H₂₀N₂O
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structural framework is particularly valuable in the development of compounds targeting the central nervous system, including potential treatments for neurological disorders such as depression, anxiety, and schizophrenia. Additionally, its carbazole core is often explored for its potential anti-inflammatory and anticancer properties, making it a subject of interest in drug discovery and development research. The dimethylamino group further enhances its reactivity, allowing for modifications that can lead to the creation of novel therapeutic agents with improved efficacy and selectivity.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,500.00
inventory 25mg
10-20 days ฿6,500.00
inventory bulk
10-20 days ฿0.00
inventory 50mg
10-20 days ฿11,000.00
3-[(Dimethylamino)methyl]-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structural framework is particularly valuable in the development of compounds targeting the central nervous system, including potential treatments for neurological disorders such as depression, anxiety, and schizophrenia. Additionally, its carbazole core is often explored for its potential anti-inflammatory and anticancer properties, making it a subject of interest in drug discovery and development research. The dimethylamino group further enhances its reactivity, allowing for modifications that can lead to the creation of novel therapeutic agents with improved efficacy and selectivity.
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