2-Furanacrolein

2-Furanacrolein
  • CAS No.:623-30-3
Other grades of this product :
2-Furanacrolein Basic information
Product Name:2-Furanacrolein
Synonyms:B-(2-FURFURYLIDENE)ACETALDEHYDE;B-(2-FURYL)ACROLEIN;BETA-(2-FURYLACROLEIN) TRANS-ISOMER;(E)-3-FURAN-2-YL-PROPENAL;FURAN-2-ACROLEIN;FURYL ACROLEIN;FEMA 2494;AKOS BBS-00003241
CAS:623-30-3
MF:C7H6O2
MW:122.12
EINECS:210-785-3
Product Categories:Alphabetical Listings;E-F;Heterocycles;Furan&Benzofuran;aldehyde Flavor;Flavors and Fragrances
Mol File:623-30-3.mol
2-Furanacrolein Chemical Properties
Melting point 49-55 °C(lit.)
Boiling point 143 °C37 mm Hg(lit.)
density 1.1483 (rough estimate)
refractive index 1.5286 (estimate)
FEMA 2494 | 3-(2-FURYL)ACROLEIN
Fp 211 °F
storage temp. 2-8°C
form powder to crystal
color White to Light yellow to Dark green
Water Solubility insoluble
Sensitive Air Sensitive
JECFA Number1497
BRN 107570
CAS DataBase Reference623-30-3(CAS DataBase Reference)
NIST Chemistry Reference2-Propenal, 3-(2-furanyl)-(623-30-3)
EPA Substance Registry System2-Propenal, 3-(2-furanyl)- (623-30-3)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-27-28-36/37/39-45-24/25
RIDADR UN 1759 8/PG 2
WGK Germany 3
RTECS LT8528500
TSCA Yes
HazardClass 8
PackingGroup III
HS Code 29321900
MSDS Information
ProviderLanguage
3-(2-Furyl)acrylaldehyde English
SigmaAldrich English
ACROS English
ALFA English
2-Furanacrolein Usage And Synthesis
Chemical PropertiesColorless to light yellow liqui
Chemical Properties3(2-Furyl)acrolein has a cooked spicy-herb odor and taste.
OccurrenceReported found in ground and roasted coffee and rum
Synthesis Reference(s)The Journal of Organic Chemistry, 58, p. 2517, 1993 DOI: 10.1021/jo00061a027
General DescriptionLight brown powder. Cinnamon odor.
Air & Water ReactionsInsoluble in water.
Reactivity Profile2-Furanacrolein 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.
Fire HazardFlash point data are not available for 2-Furanacrolein, but 2-Furanacrolein is probably combustible.
2-Furanacrolein Preparation Products And Raw materials

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