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Catalog Number:
26946
CAS Number:
98-03-3
2-tiofenoaldehído
Purity:
≥ 99% (GC)
Synonym(s):
Tienil-2-aldehído, 2-Tenaldehído
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Product Information

2-Thiophenealdehyde is a versatile compound widely recognized for its unique aromatic properties and functional group, making it a valuable asset in various chemical applications. This compound, also known as thiophene-2-carbaldehyde, features a thiophene ring with an aldehyde functional group, which enhances its reactivity and allows for diverse synthetic pathways. Researchers and industry professionals utilize 2-Thiophenealdehyde in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its ability to participate in electrophilic aromatic substitutions and other reactions. Its distinct structure not only contributes to the development of novel compounds but also plays a crucial role in the creation of specialty chemicals that exhibit unique properties.

In addition to its synthetic utility, 2-Thiophenealdehyde is employed in the production of dyes and pigments, where its thiophene moiety imparts stability and colorfastness. The compound's favorable characteristics, such as its moderate volatility and solubility in organic solvents, make it an ideal candidate for various applications in organic synthesis and material science. With its broad range of uses, 2-Thiophenealdehyde stands out as a key ingredient for researchers and manufacturers looking to innovate and enhance their product offerings.

Synonyms
Tienil-2-aldehído, 2-Tenaldehído
CAS Number
98-03-3
Purity
≥ 99% (GC)
Molecular Formula
C5H4OS
Molecular Weight
112.15
MDL Number
MFCD00005429
PubChem ID
7364
Appearance
Líquido de color amarillo claro a marrón claro.
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Tienil-2-aldehído, 2-Tenaldehído
CAS Number
98-03-3
Purity
≥ 99% (GC)
Molecular Formula
C5H4OS
Molecular Weight
112.15
MDL Number
MFCD00005429
PubChem ID
7364
Appearance
Líquido de color amarillo claro a marrón claro.
Conditions
Conservar entre 0 y 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-Thiophenealdehyde is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various heterocyclic compounds, which are essential in pharmaceuticals and agrochemicals.
  • Material Science: It is used in the development of conductive polymers and organic semiconductors, contributing to advancements in electronic materials.
  • Flavor and Fragrance Industry: 2-Thiophenealdehyde is employed in creating specific aroma compounds, enhancing the sensory qualities of perfumes and food products.
  • Analytical Chemistry: This chemical acts as a reagent in various analytical techniques, aiding in the detection and quantification of other compounds.
  • Research on Biological Activity: Studies have indicated its potential in exhibiting antimicrobial and antifungal properties, making it a candidate for further exploration in medicinal chemistry.

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