Molecular Formula: C6H5ClO
Molecular weight: 128.5563
InChi: InChI=1S/C6H5ClO/c7-5-1-3-6(8)4-2-5/h1-4,8H
InChi Key: WXNZTHHGJRFXKQ-UHFFFAOYSA-N
SMILES: c1(ccc(cc1)O)Cl
Chemical Name
4-chloro-phenol
4-Cl-phenol
p-chlorophenol
p-Cl-C6H4-OH
p-monochlorophenol
para-chloro-phenol
4-chloro-phenol
4-Cl-phenol
p-chlorophenol
p-Cl-C6H4-OH
p-monochlorophenol
para-chloro-phenol

Pytela, Oldrich
Padelkova, Zdenka
Cibulka, Radek
Kotoucova, Hana
Dvorakova, Hana
Strnadova, Iveta
Kovandova, Martina
Chudoba, Josef
Hanusek, Jiri
Kavalek, Jaromir
Hejtmankova, Ludmila
Sterba, Vojeslav
Beier, Petr
Mindl, Jaromir
Ponomarov, Oleksandr
DUSEK, Libor
Strakova, Helena
Hrabik, Oldrich
Williams, Andrew
Bahnik, Zdenek
Padelkova, Zdenka
Cibulka, Radek
Kotoucova, Hana
Dvorakova, Hana
Strnadova, Iveta
Kovandova, Martina
Chudoba, Josef
Hanusek, Jiri
Kavalek, Jaromir
Hejtmankova, Ludmila
Sterba, Vojeslav
Beier, Petr
Mindl, Jaromir
Ponomarov, Oleksandr
DUSEK, Libor
Strakova, Helena
Hrabik, Oldrich
Williams, Andrew
Bahnik, Zdenek

Cibulka, Radek;
Kotoucova, Hana;
Dvorakova, Hana;
Strnadova, Iveta;
Kovandova, Martina;
Chudoba, Josef, Biomimetic aerobic oxidative hydroxylation of arylboronic acids to phenols catalysed by a flavin derivative. Organic and Biomolecular Chemistry 2014, 12(13), 2137 - 2142, 10.1039/c3ob42081g
.

Hanusek, Jiri;
Sterba, Vojeslav;
Beier, Petr;
Mindl, Jaromir, Kinetics and mechanism of base-catalysed degradations of substituted aryl-N-hydroxycarbamates, their N-methyl and N-phenyl analogues. Organic and Biomolecular Chemistry 2004, 2(4), 562 - 569, 10.1039/b310454k
.

Padelkova, Zdenka;
Hanusek, Jiri;
Ponomarov, Oleksandr, Synthesis and structure of substituted 5-phenoxy-1,2,4-dithiazole-3-ones. Journal of Heterocyclic Chemistry 2011, 48(6), 1225 - 1228, 10.1002/jhet.717
.

Kavalek, Jaromir;
Hejtmankova, Ludmila;
Sterba, Vojeslav, KINETICS AND MECHANISM OF SOLVOLYSIS OF SUBSTITUTED PHENYL N-PHENYLBENZIMIDOESTERS. Collect. Czech. Chem. Commun. 1987, 52(5), 1285 - 1297.
Kavalek, Jaromir;
Sterba, Vojeslav;
DUSEK, Libor, Kinetics of methanolysis of substituted benzamide O-(phenoxycarbonyl)- and O-(alkoxycarbonyl)oximes catalyzed by sodium methanolate. Collect. Czech. Chem. Commun. 1999, 64(2), 265 - 287.
Kavalek, Jaromir;
Sterba, Vojeslav;
Mindl, Jaromir;
Strakova, Helena, Kinetics of base-catalysed hydrolysis and cyclisation of substituted acetamide and benzamide O-(phenoxycarbonyl)oximes. Collect. Czech. Chem. Commun. 1999, 64(10), 1641 - 1653.
Kavalek, Jaromir;
Sterba, Vojeslav;
Mindl, Jaromir;
Hrabik, Oldrich;
Williams, Andrew, The base-catalysed cyclisation of phenyl N-(2-hydroxybenzyl)-N-methylcarbamates is concerted. Organic and Biomolecular Chemistry 2003, 1(2), 415 - 421, 10.1039/b209323p
.
