Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H5O4S.Na.2H2O |
| Molecular Weight | 232.187 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.[Na+].OC1=C(C=CC=C1)S([O-])(=O)=O
InChI
InChIKey=CWWOYOYDRAZHKX-UHFFFAOYSA-M
InChI=1S/C6H6O4S.Na.2H2O/c7-5-3-1-2-4-6(5)11(8,9)10;;;/h1-4,7H,(H,8,9,10);;2*1H2/q;+1;;/p-1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Considerable change of fluorescence properties upon multiple binding of coralyne to 4-sulfonatocalixarenes. | 2010-03-04 |
|
| Preparation of phenolic compounds by decarboxylation of hydroxybenzoic acids or desulfonation of hydroxybenzenesulfonic acid, catalysed by electron rich palladium complexes. | 2009-06-28 |
|
| Formation of a liquid organic ion associate in aqueous solution and its application to the GF-AAS determination of trace cadmium in environmental water as a complex with 2-(5-bromo-2-pyridylazo)-5-(N-propyl-N-sulfopropylamino)phenol. | 2008-07 |
|
| Formation of drug-arylsulfonate complexes inside liposomes: a novel approach to improve drug retention. | 2006-01-10 |
|
| A skin sensitization safety assessment of a new bleach activator technology in detergent applications. | 2002-04 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
23718305
Created by
admin on Wed Apr 02 16:47:00 GMT 2025 , Edited by admin on Wed Apr 02 16:47:00 GMT 2025
|
PRIMARY | |||
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F6ZYN1R20Z
Created by
admin on Wed Apr 02 16:47:00 GMT 2025 , Edited by admin on Wed Apr 02 16:47:00 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
