Detail of compound @ czechem

Molecular Formula: C₃H₆O₂

Molecular weight: 74.07854

InChi: InChI=1S/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3

InChi Key: WBJINCZRORDGAQ-UHFFFAOYSA-N

SMILES: O(CC)C=O

Chemical Name
Areginal
ethyl formate
ethyl formiate
ethyl ortho-formate
EtO-CHO
formic acid ethyl ester
HC(O)OEt

External Links
PubChem

Authors of compound

Bures, Filip
Kulhanek, Jiri
Bernd Schweizer
Simon, Petr
Holy, Antonin
Masojidkova, Milena
Hrebabecky, Hubert
Sala, Michal
Luebbers, Thomas
Angehrn, Peter
Gmuender, Hans
Herzig, Silvia
Kulhanek, Josef
Mazal, Ctibor
Rothova, Vera
Jonas, Jaroslav
Melsa, Petr

Articles

Bures, Filip; Kulhanek, Jiri; Bernd Schweizer; Simon, Petr, Utilizing terpene derivatives in the synthesis of annulated terpene-imidazoles with application in the nitroaldol reaction. Tetrahedron Asymmetry 2008, 19(21), 2462 - 2469, 10.1016/j.tetasy.2008.10.026

Holy, Antonin; Masojidkova, Milena; Hrebabecky, Hubert; Sala, Michal, Synthesis of racemic 2-hydroxy-4- and 2-hydroxy-5-(hydroxymethyl) cyclohexane pyrimidine C-Nucleoside analogues. Collect. Czech. Chem. Commun. 2004, 69(4), 918 - 932, 10.1135/cccc20040918

Luebbers, Thomas; Angehrn, Peter; Gmuender, Hans; Herzig, Silvia; Kulhanek, Josef, Design, synthesis, and structure - Activity relationship studies of ATP analogues as DNA gyrase inhibitors. Bioorganic and Medicinal Chemistry Letters 2000, 10(8), 821 - 826, 10.1016/S0960-894X(00)00109-8

Mazal, Ctibor; Rothova, Vera; Jonas, Jaroslav, SODIUM SALT, SULFONATES AND CARBOXYLATES OF (E)- AND (Z)-3-(HYDROXYMETHYLENE)-5-METHYLDIHYDRO-2(3H)-FURANONE. Collect. Czech. Chem. Commun. 1985, 50(2), 348 - 356.

Mazal, Ctibor; Jonas, Jaroslav, SULPHONATES AND CARBOXYLATES OF (E)- AND (Z)-3-(HYDROXYMETHYLENE)-trans-HEXAHYDRO-2(3H)-BENZOFURANONE. Collect. Czech. Chem. Commun. 1987, 52(1), 199 - 206.

Mazal, Ctibor; Jonas, Jaroslav, NUCLEOPHILIC VINYLIC SUBSTITUTION ON α-TOSYLOXYMETHYLLENE LACTONES. Collect. Czech. Chem. Commun. 1993, 58(7), 1607 - 1623, 10.1135/cccc19931607

Mazal, Ctibor; Melsa, Petr, π-facial selectivity in 1,3-dipolar cycloaddition reactions of α-methylidene-γ-lactone substituted by 4-methyl-2,6,7-trioxabicyclo[2.2.2]Octan-1-yl group in γ-position. Collect. Czech. Chem. Commun. 2002, 67(3), 353 - 364, 10.1135/cccc20020353