Thiazole-4-carbaldehyde

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Reagent Code: #242967
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CAS Number 3364-80-5

science Other reagents with same CAS 3364-80-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 113.14 g/mol
Formula C₄H₃NOS
badge Registry Numbers
MDL Number MFCD00626896
thermostat Physical Properties
Melting Point 60-64 °C
Boiling Point 222.4 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Thiazole-4-carbaldehyde is primarily used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its aldehyde functional group allows for easy modification, making it valuable in constructing heterocyclic systems found in drugs. It is commonly employed in the development of antimicrobial, antifungal, and anti-inflammatory agents. Additionally, it serves as a building block in the preparation of thiazole-based dyes and functional materials. Its reactivity supports use in condensation reactions, such as Knoevenagel or Wittig, to extend conjugation for optoelectronic materials. It also finds application in agrochemical synthesis, contributing to the creation of novel pesticides and herbicides with improved efficacy.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,280.00
inventory 1g
10-20 days ฿970.00

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Thiazole-4-carbaldehyde
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Thiazole-4-carbaldehyde is primarily used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its aldehyde functional group allows for easy modification, making it valuable in constructing heterocyclic systems found in drugs. It is commonly employed in the development of antimicrobial, antifungal, and anti-inflammatory agents. Additionally, it serves as a building block in the preparation of thiazole-based dyes and functional materials. Its reactivity supports use

Thiazole-4-carbaldehyde is primarily used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its aldehyde functional group allows for easy modification, making it valuable in constructing heterocyclic systems found in drugs. It is commonly employed in the development of antimicrobial, antifungal, and anti-inflammatory agents. Additionally, it serves as a building block in the preparation of thiazole-based dyes and functional materials. Its reactivity supports use in condensation reactions, such as Knoevenagel or Wittig, to extend conjugation for optoelectronic materials. It also finds application in agrochemical synthesis, contributing to the creation of novel pesticides and herbicides with improved efficacy.

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