5-Acetylthiophene-2-carbaldehyde

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Reagent Code: #135685
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CAS Number 4565-29-1

science Other reagents with same CAS 4565-29-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.19 g/mol
Formula C₇H₆O₂S
thermostat Physical Properties
Melting Point 104-105°C
Boiling Point 307.4°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its aldehyde and acetyl functional groups allow for versatile chemical modifications, making it valuable in creating heterocyclic compounds with potential antimicrobial, anti-inflammatory, or antitumor activities. Also employed in the preparation of organic semiconductors and fluorescent dyes due to the electron-rich nature of the thiophene ring, which supports conjugation and charge transport in optoelectronic materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,370.00
inventory 1g
10-20 days ฿7,480.00

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5-Acetylthiophene-2-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its aldehyde and acetyl functional groups allow for versatile chemical modifications, making it valuable in creating heterocyclic compounds with potential antimicrobial, anti-inflammatory, or antitumor activities. Also employed in the preparation of organic semiconductors and fluorescent dyes due to the electron-rich nature of the thiophene ring, which

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its aldehyde and acetyl functional groups allow for versatile chemical modifications, making it valuable in creating heterocyclic compounds with potential antimicrobial, anti-inflammatory, or antitumor activities. Also employed in the preparation of organic semiconductors and fluorescent dyes due to the electron-rich nature of the thiophene ring, which supports conjugation and charge transport in optoelectronic materials.

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