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Compound - 2-methylene-4OH


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Formula: C5H10O 
CAS#: 4435-54-5 
MW: 86.13 

[MS]  [ NMR ]  [Behavioural function]  [Chemdraw

Dots surface:

Reference(s) for synthesis of 2-Methylenebutan-1-ol

Bowen, R.D., Edwards, H.G.M., Farwell, D.W., Rusike, I., and Saunders, D.M. 1998. Analytical applications of Raman spectroscopy in organic chemistry: influence of the position, stereochemistry and substitution pattern of the double bond on the (CC) and (sp2-CH) stretching bands in the Raman spectra of alkenyl methyl ethers. J. Chem. Res. 8:426-427.
Chin, C.S., Lee, B., Kim, S., and Chun, J. 1991. Generation of simple enols in non-aqueous solution by fast double-bond migration of allylic alcohols with rhodium(I) and iridium(I) complexes. J. Chem. Soc. Dalton Trans. 3:443-448.
Jahangiri, G.K., and Reymond, J.-L. 1994. Antibody-catalyzed hydrolysis of enol ethers. 2. Structure of the antibody-transition state complex and origin of the enantioselectivity. J. Am. Chem. Soc. 116:11264-11274.
Searles, S., Nickerson, R.G., Jr., Witsiepe, W.K. 1959. Oxetanes. IX. Structural and solvent effects in the reaction of gamma-bromoalcohols with base. J. Org. Chem. 24:1839-1844.

Citation: El-Sayed AM 2014. The Pherobase: Database of Insect Pheromones and Semiochemicals. <>.
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