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Compound - DEET [N,N-Diethyl-3-methylbenzamide]
 


Bedoukain RussellIPM
 
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N,N-Diethyl-3-methylbenzamide
N,N-Diethyl-3-methylbenzamide

Formula: C12H17NO 
CAS#: 134-62-3 
MW: 191.27 

[MS]  [ NMR ]  [ Kovats ]  [Behavioural function]  [Occurrence in flower





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Reference(s) for synthesis of N,N-Diethyl-3-methylbenzamide [DEET]


De Vekki, A.V., and Mozzhukhina, T.N. 1997. Pet. Chem. USSR (Engl. Transl.). 37:320-331.
 
Iwao, M., Iihama, T., Mahalanabis, K.K., Perrier, H., and Snieckus, V. 1989. Ortho-metalated aryl tert-butyl sulfones. Comparison with other directing groups and new methodology for polysubstituted aromatics. J. Org. Chem. 54:24-26.
 
Nery, M.S., Ribeiro, R.P., Lopes, C.C., and Lopes, R.S.C. 2003. Niobium pentachloride promoted conversion of carboxylic acids to carboxamides: synthesis of the 4-aryl-1,2,3,4-tetrahydroisoquinoline alkaloid­ structures. Synthesis. 2:272-276.
 
Shioiri, T., Yokoyama, Y., Kasai, Y., and Yamada, S. 1976. Phosphorus in organic synthesis - XI. Amino acids and peptides - XXI . Tetrahedron. 32:2211-2217.
 
Yamada, S.-I., Kasai, Y., and Shioiri, T. 1973. Diethylphosphoryl cyanide. A new reagent for the synthesis of amides. Tetrahedron Lett. 14:1595-1598.
 

 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
Ⓒ 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
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