2-vinyl furan

furan, 2-ethenyl-

CAS: 1487-18-9 C6 H6 O MW: 94.11302000 phenolic

Identification

Name2-vinyl furan
IUPAC2-ethenylfuran
CAS Number1487-18-9
FDA UNIIV5MN67I54D
Molecular FormulaC6 H6 O
Molecular Weight94.11302000
Nikkaji NumberJ47.979I
XlogP32.00 (est)

Regulatory

Physical Properties

Appearance colorless to pale yellow clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point -94.00 °C. @ 760.00 mm Hg
Boiling Point 99.00 to 100.00 °C. @ 760.00 mm Hg, 100.00 to 101.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 42.581001 mmHg @ 25.00 °C. (est)
Flash Point 42.00 °F. TCC ( 5.50 °C. ) (est)
logP (o/w) 2.395 (est)
Soluble in alcohol
Insoluble in water

Organoleptic Properties

Taste Description phenolic coffee grounds

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for 2-vinyl furan usage levels up tonot for fragrance use.
Recommendation for 2-vinyl furan flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

coffee roasted coffee PMC

Synonyms

2- ethenyl furan 2- ethenylfuran furan, 2-ethenyl- furan, 2-vinyl- 2- vinylfuran US Patents: 3,931,166 - Certain 2,5-dimethyl-3-thiopyrazines PubMed: Amino acid-catalyzed formation of 2-vinylfuran from lipid-derived 4-oxo-2-hexenal. PubMed: 3-[2-(3,5-Dimethoxyphenyl)vinyl]furan protects hippocampal neurons against ischemic damage. PubMed: Three-component reactions of isocyanides, dialkyl acetylenedicarboxylates, and trans-cinnamoyl chlorides for the synthesis of highly functionalized 2-vinyl furans. PubMed: Ab initio study of the decomposition of 2,5-dimethylfuran. PubMed: Formation enthalpies and bond dissociation energies of alkylfurans. The strongest CX bonds known? PubMed: Synthesis of 5-acetoxymethyl- and 5-hydroxymethyl-2-vinyl-furan. PubMed: Complete 1H and 13C NMR assignment of trans,trans-2,3-divinylfuran derivatives. PubMed: Synthesis of D- and L-deoxymannojirimycin via an asymmetric aminohydroxylation of vinylfuran. PubMed: The inhibitory effect of vinylfurans on the glycolysis in tumor and yeast cells. PubMed: Antimicrobial activity of 2-vinylfuran derivatives.