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Catalog Number:
17392
CAS Number:
3364-80-5
1,3-Thiazole-4-carboxaldehyde
Purity:
≥ 98% (HPLC)
Synonym(s):
Thiazole-4-carboxaldehyde
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Product Information

1,3-Thiazole-4-carboxaldehyde is a versatile heterocyclic compound known for its unique thiazole ring structure, which imparts significant reactivity and functionality. This compound is widely utilized in the synthesis of various pharmaceuticals and agrochemicals, serving as a key intermediate in the production of biologically active molecules. Its ability to participate in diverse chemical reactions, such as condensation and nucleophilic addition, makes it an invaluable asset in organic synthesis. Researchers and industry professionals appreciate its role in developing novel compounds with potential applications in medicinal chemistry, particularly in the design of anti-inflammatory and antimicrobial agents.

Additionally, 1,3-Thiazole-4-carboxaldehyde is recognized for its potential in the field of materials science, where it can be employed in the creation of specialized polymers and coatings. Its unique properties allow for the modification of material characteristics, enhancing performance in various applications. With its broad applicability and significant benefits, this compound stands out as a crucial building block for innovative research and development in multiple industries.

Synonyms
Thiazole-4-carboxaldehyde
CAS Number
3364-80-5
Purity
≥ 98% (HPLC)
Molecular Formula
C4H3NOS
Molecular Weight
113.14
MDL Number
MFCD00626896
PubChem ID
2763214
Appearance
Yellow Powder
Conditions
Store at 0-8°C
General Information
Synonyms
Thiazole-4-carboxaldehyde
CAS Number
3364-80-5
Purity
≥ 98% (HPLC)
Molecular Formula
C4H3NOS
Molecular Weight
113.14
MDL Number
MFCD00626896
PubChem ID
2763214
Appearance
Yellow Powder
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

1,3-Thiazole-4-carboxaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting infectious diseases and cancer. Its unique structure allows for the modification of biological activity, making it a valuable asset in drug design.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, including fungicides and herbicides. The compound's efficacy in controlling plant pathogens enhances crop yield and quality, addressing the growing demand for sustainable agricultural practices.
  • Material Science: 1,3-Thiazole-4-carboxaldehyde is employed in the development of specialty polymers and coatings. Its ability to impart unique properties, such as increased thermal stability and chemical resistance, is beneficial in industries like automotive and electronics.
  • Flavor and Fragrance Industry: This compound is utilized in the synthesis of flavoring agents and fragrances, contributing to the development of new scents and tastes. Its distinct aromatic profile can enhance product appeal in food and cosmetic applications.
  • Analytical Chemistry: It is used as a reagent in various analytical techniques, including chromatography and spectroscopy. This application aids in the detection and quantification of other compounds, providing valuable insights in research and quality control.

Citations