48190
(±)-1-(2-Furyl)ethanol
≥99.0% (GC)
Sinônimo(s):
(±)-α-Methylfuran-2-methanol, (±)-2-Furyl methyl carbinol
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About This Item
Produtos recomendados
Nível de qualidade
Ensaio
≥99.0% (GC)
contém
~0.05% hydroquinone as stabilizer
índice de refração
n20/D 1.479
p.e.
167-170 °C
densidade
1.078 g/mL at 20 °C (lit.)
grupo funcional
hydroxyl
temperatura de armazenamento
2-8°C
cadeia de caracteres SMILES
CC(O)c1ccco1
InChI
1S/C6H8O2/c1-5(7)6-3-2-4-8-6/h2-5,7H,1H3
chave InChI
UABXUIWIFUZYQK-UHFFFAOYSA-N
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Descrição geral
(±)-1-(2-Furyl)ethanol [(±)-2-Furyl methyl carbinol] is a furan derivative. The synthesis of 4-hydroxy-2-methylcyclopent-2-en-1-one from 2-furyl methyl carbinol has been reported.
Aplicação
(±)-1-(2-Furyl)ethanol (Racemic 1-(2-furyl)ethanol) may be used in the synthesis of 1-acetoxy-1-[2-furyl]ethan.
Atenção
may discolor to brown on storage
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
230.0 °F - closed cup
Ponto de fulgor (°C)
110 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves
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Chirality, 13(2), 118-123 (2001-02-15)
Asymmetric acetylation of racemic 1-(2-furyl)ethanol with the innocuous acyl donor isopropenyl acetate catalyzed by lipases in organic media afforded the chiral alcohol and acetate in high enantiomeric excess (up to 99%). The effect of molecular sieves as well as organic
An Enantioselective Total Synthetic Approach to (+)-Heptemerone G and (+)-Guanacastepene A from 2-Furyl Methyl Carbinol.
Synlett, 24, 1387-1390 (2013)
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The formation of 2-vinylfuran from the corresponding 4-oxo-2-hexenal (OHE, a lipid oxidation product) under the catalysis of amino acid were studied. The effects of amino acids, reaction temperature, reaction time, water content, pH, metallic ions and some food additives on
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