(3-Aminobenzofuran-2-yl)(3,4-dimethoxyphenyl)methanone

97%

Reagent Code: #113205
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CAS Number 733790-97-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.31 g/mol
Formula C₁₇H₁₅NO₄
badge Registry Numbers
MDL Number MFCD04636552
thermostat Physical Properties
Boiling Point 513.9±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This compound finds application in the field of medicinal chemistry, particularly in the development of bioactive molecules. It serves as a key intermediate in the synthesis of potential therapeutic agents, especially those targeting neurological disorders. The structure, featuring both benzofuran and dimethoxyphenyl groups, is often explored for its ability to interact with specific enzymes or receptors in the brain, making it valuable in the design of drugs for conditions like Alzheimer's disease or Parkinson's disease. Additionally, its unique chemical framework is utilized in research to study structure-activity relationships, aiding in the optimization of drug candidates for enhanced efficacy and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,188.00
inventory 1g
10-20 days ฿5,940.00
inventory 250mg
10-20 days ฿1,980.00
(3-Aminobenzofuran-2-yl)(3,4-dimethoxyphenyl)methanone
This compound finds application in the field of medicinal chemistry, particularly in the development of bioactive molecules. It serves as a key intermediate in the synthesis of potential therapeutic agents, especially those targeting neurological disorders. The structure, featuring both benzofuran and dimethoxyphenyl groups, is often explored for its ability to interact with specific enzymes or receptors in the brain, making it valuable in the design of drugs for conditions like Alzheimer's disease or Parkinson's disease. Additionally, its unique chemical framework is utilized in research to study structure-activity relationships, aiding in the optimization of drug candidates for enhanced efficacy and selectivity.
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