CAS 623-15-4
:Furfurylideneacetone
- (3E)-4-(furan-2-yl)but-3-en-2-one
- (3Z)-4-(furan-2-yl)but-3-en-2-one
- 1-(2-Furyl)but-1-en-3-one
- 2-(3-Oxo-1-butenyl)furan
- 2-(3-Oxobut-1-en-1-yl)furan
- 2-Furfurylideneacetone
- 3-Buten-2-one, 4-(2-furanyl)-
- 3-Buten-2-one, 4-(2-furanyl)-, (3Z)- (9CI)
- 3-Buten-2-one, 4-(2-furyl)-
- 3-Buten-2-one, 4-(2-furyl)- (6CI,8CI)
- 3-Butene-2-one, 4-(2-furanyl)-
- 4-(2-Furanyl)-3-buten-2-one
- 4-(2-Furyl)-3-Buten-2-One, Predominantly Cis
- 4-(2-Furyl)-3-butene-2-one
- 4-(2-Furyl)but-3-en-2-one
- 4-(2-Furyl)buten-2-one
- 4-(Furan-2-Yl)But-3-En-2-One
- Ai3-05777
- Ccris 6241
- FAM (monomer)
- FEMA No. 2495
- Furfural acetone
- Furfuralacetone
- Furfuryl acetone
- Furfurylidenacetone
- Furfurylideneacetone
- Monofurfurylideneacetone
- Monomer FAM
- NSC 643044
- Nsc 2065
- Nsc 6104
- See more synonyms
4-(2-Furyl)-3-buten-2-one
CAS:Formula:C8H8O2Purity:>98.0%(GC)Color and Shape:Light yellow to Brown powder to lumpMolecular weight:136.154-(2-Furyl)-3-buten-2-one, cis + trans, 98%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C8H8O2Purity:98%Color and Shape:Crystals or powder or crystalline powder or fused solid, Pale yellow to orange to brownMolecular weight:136.154-(Furan-2-yl)but-3-en-2-one
CAS:Formula:C8H8O2Purity:97%Color and Shape:SolidMolecular weight:136.14794-(2-Furyl)-3-buten-2-one
CAS:4-(2-Furyl)-3-buten-2-onePurity:98%Color and Shape:Yellow Low-Melting SolidMolecular weight:136.15g/mol4-(2-Furyl)-3-buten-2-one
CAS:Controlled ProductFormula:C8H8O2Color and Shape:NeatMolecular weight:136.152-Furfurylideneacetone
CAS:2-Furfurylideneacetone is a reactive chemical that reacts with furfuryl acetate to form cross-links. It is used as a cross-linking agent in the production of polyvinyl alcohol, polyvinyl chloride, and polyurethane elastomers. This compound has been shown to be genotoxic in the Ames test and may have mutagenic potential due to its ability to induce DNA strand breaks in bacterial cells. 2-Furfurylideneacetone is produced by reacting an unsaturated ketone with an aldehyde or other electrophiles. The reaction mechanism for this process has been determined using a flow system and viscosity measurements. The activation energy for this reaction was found to be approximately
30 kJ/mol at 25 °C.Formula:C8H8O2Purity:Min. 95%Molecular weight:136.15 g/molRef: 3D-FF01125
Discontinued product






