Detail of compound @ czechem

Molecular Formula: C₇H₄Cl₂O₂

Molecular weight: 191.01146

InChi: InChI=1S/C7H4Cl2O2/c8-5-2-1-3-6(4-5)11-7(9)10/h1-4H

InChi Key: JLOMCWVILURSQX-UHFFFAOYSA-N

SMILES: c1(cc(ccc1)Cl)OC(=O)Cl

Chemical Name
3-chlorobenzyloxycarbonyl chloride
3-chlorophenyl chloroformate
m-chlorophenyl chloroformate
m-Chlorphenylchlorformiat

External Links
PubChem

Sedlak, Milos
Hanusek, Jiri
Simunek, Petr
Jansa, Petr
Kavalek, Jaromir
Sterba, Vojeslav
Beier, Petr
Mindl, Jaromir
DUSEK, Libor
Hrabik, Oldrich

Articles

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

Sedlak, Milos; Hanusek, Jiri; Jansa, Petr; Sterba, Vojeslav, Study of ring closure reaction of substituted phenyl N-(2- thiocarbamoylphenyl)carbamates catalysed by methoxide ion. J. Phys. Org. Chem. 2006, 19(1), 61 - 67, 10.1002/poc.999

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; Hrabik, Oldrich, Cyclization of substituted phenyl N-(2-hydroxybenzyl)carbamates in aprotic solvents. Synthesis of 4H-1,3-benzoxazin-2(3H)-ones. Collect. Czech. Chem. Commun. 2000, 65(8), 1262 - 1272.

Simunek, Petr; Kavalek, Jaromir; Mindl, Jaromir; Hrabik, Oldrich, Synthesis of substituted phenyl N-(2-hydroxybenzyl)-N-methyl-carbamates. Molecules 2002, 7(2), 200 - 205.

Sterba, Vojeslav; Mindl, Jaromir, KINETICS AND MECHANISM OF HYDROLYSIS OF ARYL N-METHOXYCARBAMATES AND THEIR DERIVATIVES. Collect. Czech. Chem. Commun. 1983, 48(3), 900 - 905.