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2-Furanacrolein

Product Name2-Furanacrolein
CAS623-30-3
MFC7H6O2
MW122.12
EINECS210-785-3
MOL File623-30-3.mol

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
Flash point	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
Odor Type	spicy
biological source	synthetic
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	2-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	TSCA listed
HazardClass	8
PackingGroup	III
HS Code	29321900
Storage Class	8A - Combustible corrosive hazardous materials
Hazard Classifications	Acute Tox. 4 Oral Eye Dam. 1 Skin Corr. 1B

MSDS

Provider	Language
3-(2-Furyl)acrylaldehyde	English
SigmaAldrich	English
ACROS	English
ALFA	English

Usage And Synthesis

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

General Description

Light brown powder. Cinnamon odor.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

2-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 Hazard

Flash point data are not available for 2-Furanacrolein, but 2-Furanacrolein is probably combustible.

2-Furanacrolein

Chemical Properties

Safety Information

MSDS

Usage And Synthesis

Preparation Products And Raw materials

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