3-(2-Furyl)acrolein
Grundinformationen
- CAS
39511-08-5- Standard-SMILES
O=CC=Cc1ccco1- InChIKey
VZIRCHXYMBFNFD-UHFFFAOYSA-N- Summenformel
- C7H6O2
- Durchschnittliche Molmasse
- 122,12 g/mol
- Monoisotopische Masse
- 122,03677943
Überblick
Beta-(2-furyl)acrolein is a light brown powder. Cinnamon odor. (NTP, 1992)
Namen und Bezeichner
- Bevorzugter Name
- 3-(2-Furyl)acrolein
- IUPAC
- 3-(furan-2-yl)prop-2-enal
- Englischer Name
- 3-(2-FURYL)ACROLEIN
- Summenformel
- C7H6O2
- Molmasse
- 122.12
Namen und Synonyme
3-(2-Furyl)acrolein3-(2-Furyl)acrylaldehydeDTXSID20253493-(2-Furyl)-2-propenalRefChem:1066533DTXCID905349628-201-42-Propenal, 3-(2-furanyl)-623-30-3Furyl acroleinFurfuryliden-acetaldehyd3-(2-furyl)prop-2-enal
Weitere Namen anzeigen
FEMA 2494(E)-3-(furan-2-yl)acrylaldehydeAT-511022-FURYL ACROLEINFURAN-2-ACROLEINAKOS BBS-00003241B-(2-FURYL)ACROLEINTIMTEC-BB SBB004286
beta-(2-FURYL)ACROLEIN3-(2-Furanyl)-2-propenal3-(2-furyl)-acroleinSCHEMBL560500SCHEMBL1485961AKOS025243212SB60942NCI60_001734
Datenbank-Bezeichner
- CAS
39511-08-5、623-30-3- PubChem CID
- 12174
- DTXSID
DTXSID2025349- EC Number
- 210-785-3、628-201-4
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,1
- Polarare Oberfläche (TPSA)
- 30,2 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 9
- Formalladung
- 0
- Komplexität
- 118
Experimentelle und physikochemische Eigenschaften
SpringerMaterials PropertiesBoiling point
LogP1.15
Food AdditivesFLAVORING AGENT OR ADJUVANT -> FDA Substance added to food
Flavoring AgentsEU Flavoring substances
Solubility
Insoluble (<1 mg/ml at 68.0 °F) (NTP, 1992)
Insoluble in water
Soluble (in ethanol)
Boiling Point275 °F at 14 mmHg (NTP, 1992)
Melting Point129 °F (NTP, 1992)
Physical Description
Beta-(2-furyl)acrolein is a light brown powder. Cinnamon odor. (NTP, 1992)
White or yellow needles; Cooked spicy-herb aroma
Physikochemische Eigenschaften
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
GHS-Klassifizierung
GHS Classification
This chemical does not meet GHS hazard criteria for 6.2% (88 of 1419) of reports.
Danger
H302 (93.7%): Harmful if swallowed [Warning Acute toxicity, oral]
P260, P264, P270, P280, P301+P317, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P330, P363, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 1419 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Danger
Gefahrenhinweise
Regulatory Information
Chemical: 2-Propenal, 3-(2-furanyl)-
Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)
2-Propenal, 3-(2-furanyl)-: Does not have an individual approval but may be used under an appropriate group standard
DOT LabelCorrosive
Fire HazardsFlash point data are not available for this chemical, but it is probably combustible. (NTP, 1992)
Health HazardsSYMPTOMS: Symptoms of exposure to this compound may include irritation of the eyes, skin and mucous membranes.
Reactive GroupAldehydes
Reactivity Profile
BETA-(2-FURYL)ACROLEIN 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.
Chemie und Industrie
Verwendung und Herstellung
Use Classification
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
Flavoring Agents -> JECFA Flavorings Index
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
General Manufacturing Information2-Propenal, 3-(2-furanyl)-: ACTIVE
Anwendungen
Verwenden(E)-3-(Furan-2-yl)acrylaldehyde is a useful reagent in the synthesis of highly substituted tetrahydrofurans and tetrahydropyrans using double Michael addition strategy. A synthesis intermediate.
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