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Home Other Building Blocks 1,1-Diethoxyethene

1,1-Diethoxyethene

CAS No.:
2678-54-8
Catalog Number:
AG0037H4
Molecular Formula:
C6H12O2
Molecular Weight:
116.1583
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Product Description
Catalog Number:
AG0037H4
Chemical Name:
1,1-Diethoxyethene
CAS Number:
2678-54-8
Molecular Formula:
C6H12O2
Molecular Weight:
116.1583
MDL Number:
MFCD00467747
IUPAC Name:
1,1-diethoxyethene
InChI:
InChI=1S/C6H12O2/c1-4-7-6(3)8-5-2/h3-5H2,1-2H3
InChI Key:
VTGIVYVOVVQLRL-UHFFFAOYSA-N
SMILES:
CCOC(=C)OCC
Properties
Complexity:
60.9  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
116.084g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
116.16g/mol
Monoisotopic Mass:
116.084g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
18.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.7  
Literature
Title Journal
Lewis acid catalyzed inverse-electron-demand Diels-Alder reaction of tropones. Journal of the American Chemical Society 20091125
An ion/molecule reaction for the identification of analytes with two basic functional groups. Journal of the American Society for Mass Spectrometry 20090701
Catalytic synthesis of (E)-alpha,beta-unsaturated esters from aldehydes and 1,1-diethoxyethylene. Beilstein journal of organic chemistry 20090101
Photochemical cycloaddition of mono-, 1,1-, and 1,2-disubstituted olefins to a chiral 2(5H)-furanone. Diastereoselective synthesis of (+)-lineatin. The Journal of organic chemistry 20080801
Stereoselective route to oxetanocin carbocyclic analogues based on a [2 + 2] photocycloaddition to a chiral 2(5H)-furanone. Organic letters 20070719
[2 + 2]-Photocycloaddition of 1,1-diethoxyethylene to chiral polyfunctional 2-cyclohexenones. Regioselectivity and pi-facial discrimination. The Journal of organic chemistry 20040220
Reactivity of 2-acylaminoacrylates with ketene diethyl acetal; [2 + 2] cycloadditions vs. tandem condensations. Chemical communications (Cambridge, England) 20030621
Properties