2-Methoxypropene

2-Methoxypropene
Names
	Preferred IUPAC name 2-Methoxyprop-1-ene
	Other names Methyl isopropenyl ether; Isopropenyl methyl ether
Identifiers
CAS Number	116-11-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	7999;
ECHA InfoCard	100.003.751
PubChem CID	8300;
UNII	15WBG0JT6B ;
CompTox Dashboard (EPA)	DTXSID3051591 ;
	InChI InChI=1S/C4H8O/c1-4(2)5-3/h1H2,2-3H3 Key: YOWQWFMSQCOSBA-UHFFFAOYSA-N; InChI=1/C4H8O/c1-4(2)5-3/h1H2,2-3H3 Key: YOWQWFMSQCOSBA-UHFFFAOYAD;
	SMILES CC(=C)OC;
Properties
Chemical formula	C4H8O
Molar mass	72.107 g·mol−1
Appearance	Colorless liquid
Density	0.753 g/mL
Boiling point	34 to 36 °C (93 to 97 °F; 307 to 309 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

2-Methoxypropene is an ether with the chemical formula C₄H₈O. It is a reagent used in organic synthesis to introduce a protecting group for alcohols,^[1] and the conversion diols to the acetonide group.^[3]

2-Methoxypropene can be prepared by the elimination of methanol from dimethoxypropane,^[4] or by the addition of methanol to propyne or allene.^[5]

References

1 2 Whitaker, K. Sinclair; Whitaker, D. Todd (2001). "2-Methoxypropene". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rm124. ISBN 0471936235.
1 2 2-Methoxypropene at Sigma-Aldrich
↑ Theodora W. Greene; Peter G. M. Wuts. Protective Groups in Organic Synthesis (3rd ed.). pp. 207–215.
↑ Newman, Melvin S.; Vander Zwan, Michael C. (1973). "Improved synthesis of 2-methoxypropene". The Journal of Organic Chemistry. 38 (16): 2910. doi:10.1021/jo00956a040.
↑ Agré, B. A.; Taber, A. M.; Beregovykh, V. V.; Klebanova, F. D.; Nekrasov, N. V.; Sobolev, O. B.; Kalechits, I. V. (1983). "Kinetics of the catalytic synthesis of 2-methoxypropene". Pharmaceutical Chemistry Journal. 17 (3): 221. doi:10.1007/BF00765172. S2CID 22506880.