![]() 1-氯-4-碘丁烷结构式
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常用名 | 1-氯-4-碘丁烷 | 英文名 | 1-Chloro-4-iodobutane |
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CAS号 | 10297-05-9 | 分子量 | 218.464 | |
密度 | 1.8±0.1 g/cm3 | 沸点 | 193.6±8.0 °C at 760 mmHg | |
分子式 | C4H8ClI | 熔点 | 93 °C | |
MSDS | 中文版 美版 | 闪点 | 70.9±18.4 °C | |
符号 |
![]() GHS07 |
信号词 | Warning |
Radical reactions with 3H-quinazolin-4-ones: synthesis of deoxyvasicinone, mackinazolinone, luotonin A, rutaecarpine and tryptanthrin.
Org. Biomol. Chem. 5(1) , 103-13, (2007) Alkyl, aryl, heteroaryl and acyl radicals have been cyclised onto the 2-position of 3H-quinazolin-4-one. The side chains containing the radical precursors were attached to the nitrogen atom in the 3-position. The cyclisations take place by aromatic homolytic ... |
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The synthesis of unsaturated fatty acids.
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Homogeneous catalytic reduction of a, ?-dihaloalkanes with electrogenerated nickel (I) salen. Mubarak MS and Peters DG.
J. Electroanal. Chem. 388(1) , 195-98, (1995)
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Electrochemical reduction of 1, 4-dihalobutanes at carbon cathodes in dimethylformamide. Pritts WA and Peters DG.
J. Electroanal. Chem. 380(1) , 147-160, (1995)
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Studies directed towards asymmetric synthesis of levobupivacaine. Kumar S and Ramachandran U.
Tetrahedron Lett. 46(1) , 19-21, (2005)
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