About This Item
Fórmula linear:
C6H5(CH2)4OH
Número CAS:
Peso molecular:
150.22
Beilstein:
2042122
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
99%
Formulário
liquid
índice de refração
n20/D 1.521 (lit.)
p.e.
140-142 °C/14 mmHg (lit.)
densidade
0.984 g/mL at 20 °C (lit.)
grupo funcional
hydroxyl
phenyl
cadeia de caracteres SMILES
OCCCCc1ccccc1
InChI
1S/C10H14O/c11-9-5-4-8-10-6-2-1-3-7-10/h1-3,6-7,11H,4-5,8-9H2
chave InChI
LDZLXQFDGRCELX-UHFFFAOYSA-N
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Descrição geral
4-Phenyl-1-butanol is oxidized by ceric ammonium nitrate in acetonitrile to afford 2-phenyltetrahydrofuran. It undergoes cyclization in presence of phosphoric acid at high temperature to yield tetralin.
Aplicação
4-Phenyl-1-butanol was used in synthesis of NK105, a paclitaxel-incorporating micellar nanoparticle formulation.
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, multi-purpose combination respirator cartridge (US)
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T Hamaguchi et al.
British journal of cancer, 92(7), 1240-1246 (2005-03-24)
Paclitaxel (PTX) is one of the most effective anticancer agents. In clinical practice, however, high incidences of adverse reactions of the drug, for example, neurotoxicity, myelosuppression, and allergic reactions, have been reported. NK105, a micellar nanoparticle formulation, was developed to
New Friedel-Crafts chemistry. XIX. Cyclialkylations of some phenylalkanols.
Khalaf AA and Roberts RM.
The Journal of Organic Chemistry, 34(11), 3571-3574 (1969)
Fabrice Gritti et al.
Journal of chromatography. A, 1524, 108-120 (2017-10-11)
A twin-column recycling separation process (TCRSP) is assembled and used to generate higher speed and/or higher resolution levels than those of the usual non-recycling process at the same back pressure. It enables the users to solve very challenging separation problems
Cyclic ether formation in oxidations of primary alcohols by cerium (IV). Reactions of 5-phenyl-1-pentanol, 4-phenyl-1-butanol, and 3-phenyl-1-propanol with ceric ammonium nitrate.
Doyle MP, et al.
The Journal of Organic Chemistry, 40(10), 1454-1456 (1975)
Min Kyung Song et al.
Journal of agricultural and food chemistry, 67(7), 2028-2035 (2019-01-31)
Caffeic acid phenethyl ester (CAPE) is an ester of a hydroxycinnamic acid (phenylpropanoid) and a phenylethanoid (2-phenylethanol; 2-PE), which has long been used in traditional medicine. Here, we synthesized 54 hydroxycinnamic acid-phenylethanoid esters by feeding 64 combinations of hydroxycinnamic acids
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