Molecular Formula: C7H6O2
Molecular weight: 122.12134
InChi: InChI=1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)
InChi Key: WPYMKLBDIGXBTP-UHFFFAOYSA-N
SMILES: c1(C(=O)O)ccccc1
Chemical Name
benzene carboxylic acid
benzenecarboxylic acid
benzenemonocarboxylic acid
benzoic acid
carboxybenzene
PhCO2H
phenylcarboxylic acid
benzene carboxylic acid
benzenecarboxylic acid
benzenemonocarboxylic acid
benzoic acid
carboxybenzene
PhCO2H
phenylcarboxylic acid
Authors of compound
Kulhanek, Jiri
Pytela, Oldrich
Ludwig, Miroslav
Hrdina, Radim
Budesinsky, Milos
Kavalek, Jaromir
Sterba, Vojeslav
Lycka, Antonin
Boehm, Stanislav
Oliveira-Campos, Ana M.F.
Rodrigues, Ligia M.
Esteves, Ana P.
Mueller, Christian E.
Schreiner, Peter R.
Pinto, Tiago A.D.
Kirsch, Gilbert
Fiedler, Pavel
Exner, Otto
Potesil, Tomas
Vecera, Miroslav
Novak, Jaroslav
Riha, Vaclav
Cigler, Petr
Baron, Vaclav
Kalfus, Karel
Bauerova, Ingrid
Liska, Josef
Pytela, Oldrich
Ludwig, Miroslav
Hrdina, Radim
Budesinsky, Milos
Kavalek, Jaromir
Sterba, Vojeslav
Lycka, Antonin
Boehm, Stanislav
Oliveira-Campos, Ana M.F.
Rodrigues, Ligia M.
Esteves, Ana P.
Mueller, Christian E.
Schreiner, Peter R.
Pinto, Tiago A.D.
Kirsch, Gilbert
Fiedler, Pavel
Exner, Otto
Potesil, Tomas
Vecera, Miroslav
Novak, Jaroslav
Riha, Vaclav
Cigler, Petr
Baron, Vaclav
Kalfus, Karel
Bauerova, Ingrid
Liska, Josef
Articles
Hrdina, Radim;
Mueller, Christian E.;
Schreiner, Peter R., Kinetic resolution of trans-cycloalkane-1,2-diols via Steglich esterification. Chemical Communications 2010, 46(15), 2689 - 2690, 10.1039/c001075h 
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Hrdina, Radim;
Oliveira-Campos, Ana M.F.;
Rodrigues, Ligia M.;
Esteves, Ana P.;
Pinto, Tiago A.D.;
Kirsch, Gilbert, Synthesis of esters derived from 2,3,4-tri-O-benzyl-α-D- methylglucoside. Arkivoc 2012, 2012(6), 185 - 193.
Kavalek, Jaromir;
Sterba, Vojeslav;
Novak, Jaroslav, KINETICS OF HYDROLYSIS AND REARRANGEMENTS OF S-ACYLTHIOURONIUM SALTS. Collect. Czech. Chem. Commun. 1982, 47(10), 2702 - 2710.
Kavalek, Jaromir;
Sterba, Vojeslav;
Potesil, Tomas, CYCLIZATION KINETICS AND MECHANISM OF N-BENZOYL-N'-(1,2-DIMETHYL-3-OXO-1-BUTENYL)THIOUREA. Collect. Czech. Chem. Commun. 1983, 48(2), 578 - 585.
Kulhanek, Jiri;
Pytela, Oldrich;
Ludwig, Miroslav;
Riha, Vaclav, CHEMOMETRICAL ANALYSIS OF SUBSTITUENT EFFECTS. III. ADDITIVITY OF SUBSTITUENT EFFECTS IN DISSOCIATION OF 3,4-DISUBSTITUTED BENZOIC ACIDS IN ORGANIC SOLVENTS. Collect. Czech. Chem. Commun. 1994, 59(3), 627 - 638, 10.1135/cccc19940627 .
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Kulhanek, Jiri;
Pytela, Oldrich;
Ludwig, Miroslav, CHEMOMETRICAL ANALYSIS OF SUBSTITUENT EFFECTS IV. ADDITIVITY OF SUBSTITUENT EFFECTS IN DISSOCIATION OF 3,5-DISUBSTITUTED BENZOIC ACIDS IN ORGANIC SOLVENTS. Collect. Czech. Chem. Commun. 1994, 59(7), 1637 - 1644, 10.1135/cccc19941637 .
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Kulhanek, Jiri;
Budesinsky, Milos;
Fiedler, Pavel;
Exner, Otto, Conformation and Steric Effects in Mono- and Dimethoxybenzoic Acids. Journal of Organic Chemistry 1999, 64(10), 3513 - 3518.
Kulhanek, Jiri;
Pytela, Oldrich;
Lycka, Antonin, Chemometrical analysis of substituent effects. XIII. Comparison of substituent effects on dissociation and chemical shift in C NMR spectra of mono- and disubstituted benzoic acids. Collect. Czech. Chem. Commun. 2000, 65(1), 106 - 116.
Kulhanek, Jiri;
Budesinsky, Milos;
Boehm, Stanislav;
Exner, Otto;
Cigler, Petr, C and H nuclear magnetic resonance of methyl-substituted acetophenones and methyl benzoates: Steric hindrance and inhibited conjugation. Magn. Reson. Chem. 2004, 42(10), 844 - 851, 10.1002/mrc.1414 .
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Pytela, Oldrich;
Ludwig, Miroslav;
Vecera, Miroslav;
Baron, Vaclav;
Kalfus, Karel, DISSOCIATION CONSTANTS OF SUBSTITUTED BENZOIC ACIDS IN WATER AND IN ORGANIC SOLVENTS. Collect. Czech. Chem. Commun. 1986, 51(10), 2135 - 2142.
Ludwig, Miroslav;
Bauerova, Ingrid, Substituent effects on the base-catalysed hydrolysis of phenyl esters of ortho-substituted benzoic acids. Collect. Czech. Chem. Commun. 2001, 66(5), 770 - 784, 10.1135/cccc20010770 .
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Pytela, Oldrich;
Liska, Josef, CHEMOMETRICAL ANALYSIS OF SUBSTITUENT EFFECTS. V. ortho EFFECT. Collect. Czech. Chem. Commun. 1994, 59(9), 2005 - 2021, 10.1135/cccc19942005 .
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