![]() 4,4-二甲氧基-2-丁酮结构式
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常用名 | 4,4-二甲氧基-2-丁酮 | 英文名 | 4,4-Dimethoxy-2-butanone |
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CAS号 | 5436-21-5 | 分子量 | 132.158 | |
密度 | 1.0±0.1 g/cm3 | 沸点 | 172.1±20.0 °C at 760 mmHg | |
分子式 | C6H12O3 | 熔点 | -82 °C | |
MSDS | 中文版 美版 | 闪点 | 49.4±0.0 °C | |
符号 |
![]() GHS02 |
信号词 | Warning |
Carbonylation as a key reaction in anaerobic acetone activation by Desulfococcus biacutus.
Appl. Environ. Microbiol. 79(20) , 6228-35, (2013) Acetone is activated by aerobic and nitrate-reducing bacteria via an ATP-dependent carboxylation reaction to form acetoacetate as the first reaction product. In the activation of acetone by sulfate-reducing bacteria, acetoacetate has not been found to be an i... |
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Yamadazyma Farinosa IFO 10896-mediated reduction of 4, 4-dimethoxy-2-butanone as the key-step for the preparation of 1, 3-diols with unsymmetrical substituents. Yamazaki T, et al.
Synth. Commun. 30(16) , 3061-72, (2000)
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β-keto acetals. I. Synthesis of pyrazoles and pyrimidines and the steric inhibition of resonance in 5-alkyl-1-p-nitrophenylpyrazoles. Burness DM.
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Facile template synthesis of nickel (II) complexes of dibenzotetraaza [14] annulenes. Cutler AR, et al.
Inorg. Chem. 24(14) , 2276-81, (1985)
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2-Arylpyrazolo [1,5-a] pyrimidin-3-yl acetamides. New potent and selective peripheral benzodiazepine receptor ligands. Selleri S, et al.
BioTechnol.: Indian J. 9(10) , 2661-2671, (2001)
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