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Catalog Number:
45023
CAS Number:
67869-13-0
2,3,5-Tribromo-4-methylthiophene
Purity:
≥ 97% (GC)
Documents
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Product Information

2,3,5-Tribromo-4-methylthiophene is a specialized brominated thiophene compound known for its unique properties and versatility in various applications. This compound is recognized for its effectiveness as a building block in organic synthesis, particularly in the development of advanced materials and pharmaceuticals. Its bromine substituents enhance its reactivity, making it an excellent candidate for cross-coupling reactions, which are essential in the creation of complex organic molecules. Researchers and industry professionals utilize 2,3,5-Tribromo-4-methylthiophene in the synthesis of functionalized polymers and as a precursor in the production of electronic materials, such as organic semiconductors and photovoltaic devices.

Moreover, its distinctive thiophene structure contributes to its stability and conductivity, making it valuable in the field of materials science. The compound's ability to undergo various chemical transformations allows for the customization of properties, catering to specific application needs. This makes 2,3,5-Tribromo-4-methylthiophene a vital resource for those looking to innovate in organic chemistry and materials engineering.

CAS Number
67869-13-0
Purity
≥ 97% (GC)
Molecular Formula
C5H3Br3S
Molecular Weight
334.85
MDL Number
MFCD00130086
PubChem ID
3017801
Melting Point
31 °C
Appearance
White or colorless to yellow to orange powder to lump to clear liquid
Conditions
Store at 2 - 8 °C
General Information
CAS Number
67869-13-0
Purity
≥ 97% (GC)
Molecular Formula
C5H3Br3S
Molecular Weight
334.85
MDL Number
MFCD00130086
PubChem ID
3017801
Melting Point
31 °C
Appearance
White or colorless to yellow to orange powder to lump to clear liquid
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,3,5-Tribromo-4-methylthiophene is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of brominated thiophene derivatives, which are valuable in pharmaceuticals and agrochemicals.
  • Material Science: Its unique properties make it suitable for creating advanced materials, such as conductive polymers and organic semiconductors, which are essential in electronics and optoelectronic devices.
  • Environmental Chemistry: The compound is used in studies investigating the degradation of brominated compounds in the environment, helping researchers understand their impact and develop better waste management strategies.
  • Biological Research: It has potential applications in medicinal chemistry, particularly in the design of new drugs targeting specific biological pathways, enhancing the efficacy of treatments.
  • Analytical Chemistry: This chemical is employed as a standard in various analytical techniques, aiding in the calibration and validation of methods used to detect and quantify brominated compounds in complex mixtures.

Citations