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Catalog Number:
18566
CAS Number:
885279-11-8
2-(2-Methoxyphenyl)thiazole-4-carbaldehyde
Purity:
≥ 95% (HPLC)
Documents
$106.96 /100MG
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Product Information

2-(2-Methoxyphenyl)thiazole-4-carbaldehyde is a versatile compound with significant applications in organic synthesis and medicinal chemistry. This compound, characterized by its thiazole ring and aldehyde functional group, serves as a valuable building block in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for the synthesis of derivatives that can exhibit enhanced biological activity, making it a focal point for researchers aiming to discover new therapeutic agents.

In addition to its utility in drug development, 2-(2-Methoxyphenyl)thiazole-4-carbaldehyde has been employed in the synthesis of dyes and pigments, showcasing its relevance in the materials science sector. Its ability to undergo various chemical transformations makes it an attractive option for chemists looking to innovate in both academic and industrial settings. The compound's favorable properties, such as stability and reactivity, further enhance its appeal, providing researchers with a reliable tool for their synthetic endeavors.

CAS Number
885279-11-8
Purity
≥ 95% (HPLC)
Molecular Formula
C11H9NO2S
Molecular Weight
219.26
MDL Number
MFCD06738365
PubChem ID
53407315
Appearance
Pale yellow solid
Conditions
Store at 0-8 °C
General Information
CAS Number
885279-11-8
Purity
≥ 95% (HPLC)
Molecular Formula
C11H9NO2S
Molecular Weight
219.26
MDL Number
MFCD06738365
PubChem ID
53407315
Appearance
Pale yellow solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(2-Methoxyphenyl)thiazole-4-carbaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs.
  • Organic Synthesis: It is used in organic chemistry for creating complex molecules, enabling researchers to explore new chemical reactions and pathways.
  • Material Science: The compound can be incorporated into polymer formulations, enhancing properties such as thermal stability and mechanical strength.
  • Biological Research: It is employed in studies investigating the biological activity of thiazole derivatives, contributing to the discovery of new therapeutic agents.
  • Fluorescent Probes: This chemical is utilized in developing fluorescent probes for imaging applications, allowing for better visualization in biological studies.

Citations