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Catalog Number:
42889
CAS Number:
539-47-9
3-(2-Furyl)acrylic acid
Purity:
≥ 98% (GC)
Synonym(s):
2-Furanacrylic acid
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$113.07 /10G
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Product Information

3-(2-Furyl)acrylic acid is a versatile compound known for its unique furan ring structure, which imparts distinctive properties that are valuable in various applications. This compound is primarily utilized in the synthesis of polymers, particularly in the production of specialty coatings and adhesives. Its ability to undergo polymerization makes it an excellent candidate for creating materials with enhanced thermal stability and chemical resistance. Additionally, 3-(2-Furyl)acrylic acid serves as a building block in organic synthesis, enabling researchers to develop novel pharmaceuticals and agrochemicals.

The compound's reactivity and functional properties allow it to be employed in the formulation of UV-curable coatings, which are increasingly popular in the printing and automotive industries due to their quick drying times and durability. Furthermore, its unique structure can lead to innovative applications in the development of bioactive compounds, making it a valuable asset for researchers focused on sustainable chemistry. With its diverse range of applications, 3-(2-Furyl)acrylic acid stands out as a key ingredient for professionals seeking to enhance product performance and explore new chemical pathways.

Synonyms
2-Furanacrylic acid
CAS Number
539-47-9
Purity
≥ 98% (GC)
Molecular Formula
C7H6O3
Molecular Weight
138.12
MDL Number
MFCD00003257
PubChem ID
10876
Melting Point
140 - 143 °C
Appearance
Light orange to yellow to green crystalline powder
Boiling Point
286 °C
Conditions
Store at RT
General Information
Synonyms
2-Furanacrylic acid
CAS Number
539-47-9
Purity
≥ 98% (GC)
Molecular Formula
C7H6O3
Molecular Weight
138.12
MDL Number
MFCD00003257
PubChem ID
10876
Melting Point
140 - 143 °C
Appearance
Light orange to yellow to green crystalline powder
Boiling Point
286 °C
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(2-Furyl)acrylic acid 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 cancer and inflammation, due to its unique structural properties that enhance biological activity.
  • Polymer Chemistry: It is used in the production of specialty polymers and resins, where its furan ring contributes to improved thermal stability and mechanical properties, making it suitable for high-performance applications.
  • Food Industry: The compound can be employed as a flavoring agent or preservative, leveraging its natural origin and potential antioxidant properties to enhance food quality and shelf-life.
  • Material Science: It is utilized in the development of advanced materials, such as coatings and adhesives, where its reactivity allows for the formation of durable and resistant products.
  • Agricultural Applications: The compound shows promise in the formulation of agrochemicals, particularly as a building block for herbicides and pesticides, offering targeted action with reduced environmental impact.

Citations