产品名称
4-羟基-2-丁酮, 95%
InChI key
LVSQXDHWDCMMRJ-UHFFFAOYSA-N
InChI
1S/C4H8O2/c1-4(6)2-3-5/h5H,2-3H2,1H3
SMILES string
CC(=O)CCO
assay
95%
refractive index
n20/D 1.430 (lit.)
bp
73-76 °C/12 mmHg (lit.)
density
1.023 g/mL at 25 °C (lit.)
functional group
hydroxyl
ketone
Quality Level
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Application
4-羟基-2-丁酮已被用于合成:
- 通过锐钛矿-TiO2催化的脱水反应生成3-丁烯-2-酮
- 4-甲基-5-羟甲基噻唑
- (+/-)-3,3,7-三甲基-2,9-二氧杂三环[3.3.1.04,7]壬烷
- 甲羟戊酸内酯
- 疣孢菌素
- β-羟基内酯
General description
4-羟基-2-丁酮是一种β-羟基酮,用作合成1,3-丁二醇的起始物。
44-羟基-2-丁酮是一种重要的药物中间体。已经通过绝对速率法研究了羟自由基与4-羟基-2-丁酮的气相反应。
44-羟基-2-丁酮是一种重要的药物中间体。已经通过绝对速率法研究了羟自由基与4-羟基-2-丁酮的气相反应。
Journal of the American Chemical Society, 67, 400-400 (1945)
Gisèle El Dib et al.
The journal of physical chemistry. A, 117(1), 117-125 (2012-12-06)
The reaction of the OH radicals with 4-hydroxy-2-butanone was investigated in the gas phase using an absolute rate method at room temperature and over the pressure range 10-330 Torr in He and air as diluent gases. The rate coefficients were
Journal of the American Chemical Society, 104, 5486-5486 (1982)
Hon Wai Lam et al.
Organic letters, 7(19), 4225-4228 (2005-09-09)
[reaction: see text] Copper bisphosphine complexes catalyze the intramolecular reductive aldol reaction of alpha,beta-unsaturated esters with ketones, affording five- and six-membered beta-hydroxylactones in high stereoselectivities. Utilization of chiral nonracemic bisphosphines render the cyclizations enantioselective.
Journal of the American Chemical Society, 79, 2316-2316 (1957)
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