Detail of compound @ czechem

Molecular Formula: C₆H₅NO₃

Molecular weight: 139.1088

InChi: InChI=1S/C6H5NO3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H

InChi Key: RTZZCYNQPHTPPL-UHFFFAOYSA-N

SMILES: c1(N(=O)=O)cc(ccc1)O

Chemical Name
3-nitro-phenol
3-nitrophenol
m-hydroxynitrobenzene
m-Nitrophenol
m-NO2PhOH
meta-nitrophenol

External Links
PubChem

Authors of compound

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

Articles

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

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