cis-5-Norbornene-endo-2,3-dicarboxylic anhydride

95%

  • Product Code: 216642
  Alias:    Norbornene diacid anhydride; endomethyltetrahydrophthalic anhydride, (3aa,4a,7a,7a)-3a,4,7,7a-tetrahydro-4,7-methylene isobenzofuran-1,3-dione, 3,6-inner methylene-1,2,3,6-tetrahydrophthalic anhydride, NA anhydride
  CAS:    129-64-6
Molecular Weight: 164.16 g./mol Molecular Formula: C₉H₈O₃
EC Number: 204-957-7 MDL Number: MFCD00151106
Melting Point: 165-167 °C(lit.) Boiling Point:
Density: 1.08 Storage Condition: Room temperature, dry
Product Description: Used as a key intermediate in the synthesis of specialty polymers and resins, particularly in the production of high-performance epoxy curing agents. Its rigid norbornene structure contributes to enhanced thermal stability and mechanical strength in cured epoxy systems, making it suitable for aerospace, electronics, and advanced composite applications. Also employed in the development of functional monomers for ring-opening metathesis polymerization (ROMP), yielding polymers with tailored properties for coatings and engineering plastics. Additionally, it serves as a building block in organic synthesis for pharmaceuticals and fine chemicals due to its reactive anhydride group and well-defined stereochemistry.
Sizes / Availability / Pricing:
Size Availability Price Quantity
100g 10-20 days ฿380.00
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500g 10-20 days ฿1,460.00
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2.5kg 10-20 days ฿5,120.00
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cis-5-Norbornene-endo-2,3-dicarboxylic anhydride
Used as a key intermediate in the synthesis of specialty polymers and resins, particularly in the production of high-performance epoxy curing agents. Its rigid norbornene structure contributes to enhanced thermal stability and mechanical strength in cured epoxy systems, making it suitable for aerospace, electronics, and advanced composite applications. Also employed in the development of functional monomers for ring-opening metathesis polymerization (ROMP), yielding polymers with tailored properties for coatings and engineering plastics. Additionally, it serves as a building block in organic synthesis for pharmaceuticals and fine chemicals due to its reactive anhydride group and well-defined stereochemistry.
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