1-Chloro-4-iodobutane
1-Chloro-4-iodobutane structure
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Common Name | 1-Chloro-4-iodobutane | ||
|---|---|---|---|---|
| CAS Number | 10297-05-9 | Molecular Weight | 218.464 | |
| Density | 1.8±0.1 g/cm3 | Boiling Point | 193.6±8.0 °C at 760 mmHg | |
| Molecular Formula | C4H8ClI | Melting Point | 93 °C | |
| MSDS | Chinese USA | Flash Point | 70.9±18.4 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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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.
J. Am. Chem. Soc. 70(5) , 1699-1700., (1948)
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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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