| Identification | More | [Name]
2-Furanacrolein | [CAS]
623-30-3 | [Synonyms]
2-FURANACROLEIN
2-FURYL ACROLEIN
3-(2-FUROYL)ACROLEIN
3-(2-FURYL)ACROLEIN
3-(2-FURYL)PROPENAL
AKOS BBS-00003241
B-(2-FURFURYLIDENE)ACETALDEHYDE
B-(2-FURYL)ACROLEIN
BETA-(2-FURYLACROLEIN) TRANS-ISOMER
(E)-3-FURAN-2-YL-PROPENAL
FEMA 2494
FURAN-2-ACROLEIN
FURYL ACROLEIN
TIMTEC-BB SBB004286
TRANS-3-(2-FURYL)ACROLEIN
TRANS-BETA-(2-FURYLACROLEIN)
(2E)-3-(2-Furyl)-2-propenal
3-(2-furanyl)-2-propena
3-(2-Furanyl)-2-propenal
3-(2-Furyl)-2-propenal | [EINECS(EC#)]
210-785-3 | [Molecular Formula]
C7H6O2 | [MDL Number]
MFCD00003256 | [Molecular Weight]
122.12 | [MOL File]
623-30-3.mol |
| Chemical Properties | Back Directory | [Appearance]
Colorless to light yellow liqui | [Melting point ]
49-55 °C(lit.)
| [Boiling point ]
143 °C37 mm Hg(lit.)
| [density ]
1.1483 (rough estimate) | [FEMA ]
2494 | [refractive index ]
1.5286 (estimate) | [Fp ]
211 °F
| [storage temp. ]
2-8°C | [form ]
powder to crystal | [color ]
White to Light yellow to Dark green | [Odor]
at 1.00 % in dipropylene glycol. green grassy fruity spicy vanilla nutty woody cinnamon | [biological source]
synthetic | [Odor Type]
spicy | [Water Solubility ]
insoluble | [Sensitive ]
Air Sensitive | [JECFA Number]
1497 | [BRN ]
107570 | [Major Application]
flavors and fragrances | [Cosmetics Ingredients Functions]
PERFUMING | [InChI]
1S/C7H6O2/c8-5-1-3-7-4-2-6-9-7/h1-6H/b3-1+ | [InChIKey]
VZIRCHXYMBFNFD-HNQUOIGGSA-N | [SMILES]
[H]C(=O)\C([H])=C(/[H])c1ccco1 | [LogP]
1.74 | [CAS DataBase Reference]
623-30-3(CAS DataBase Reference) | [NIST Chemistry Reference]
2-Propenal, 3-(2-furanyl)-(623-30-3) | [EPA Substance Registry System]
623-30-3(EPA Substance) |
| Hazard Information | Back Directory | [General Description]
Light brown powder. Cinnamon odor. | [Reactivity Profile]
BETA-(2-FURYL)ACROLEIN(623-30-3) is an aldehyde. May become involved in exothermic self-condensation or polymerization reactions that are often catalyzed by acid. May generate flammable and/or toxic gases with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation. | [Air & Water Reactions]
Insoluble in water. | [Fire Hazard]
Flash point data are not available for this chemical, but BETA-(2-FURYL)ACROLEIN is probably combustible. | [Chemical Properties]
3(2-Furyl)acrolein has a cooked spicy-herb odor and taste. | [Chemical Properties]
Colorless to light yellow liqui | [Occurrence]
Reported found in ground and roasted coffee and rum | [Uses]
flavors and fragrances | [Definition]
ChEBI: 3-(2-Furanyl)-2-propenal is a heteroarene. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 58, p. 2517, 1993 DOI: 10.1021/jo00061a027 |
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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Alfa Aesar
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400-6106006 |
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http://chemicals.thermofisher.cn |
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Energy Chemical
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400-0056266 |
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www.energy-chemical.com |
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Maya High Purity Chemicals
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