Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H5ClO2 |
| Molecular Weight | 144.556 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(Cl)C(O)=C1
InChI
InChIKey=JQVAPEJNIZULEK-UHFFFAOYSA-N
InChI=1S/C6H5ClO2/c7-5-2-1-4(8)3-6(5)9/h1-3,8-9H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Photolysis of 4-chlororesorcinol in water: competitive formation of a singlet ketene and a triplet carbene. | 2010-11-14 |
|
| Monochloramination of resorcinol: mechanism and kinetic modeling. | 2009-12-15 |
|
| Examination and expansion of the substrate range of m-hydroxybenzoate hydroxylase. | 2008-06-20 |
|
| Degradation of clofibric acid in acidic aqueous medium by electro-Fenton and photoelectro-Fenton. | 2007-01 |
|
| Field-induced phase transitions and reversible field-induced inversion of chirality in tilted smectic phases of bent-core mesogens. | 2006-12 |
|
| Discrete versus infinite molecular self-assembly: control in crystalline hydrogen-bonded assemblies based on resorcinol. | 2001-11-29 |
|
| Voltammetric investigation of hair dye constituents: application to the quantification of p-phenylenediamine. | 2001-11 |
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SUBSTANCE RECORD
