Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H6O7S |
| Molecular Weight | 246.194 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC=C(C=C1C(O)=O)S(O)(=O)=O
InChI
InChIKey=WNKQDGLSQUASME-UHFFFAOYSA-N
InChI=1S/C8H6O7S/c9-7(10)5-2-1-4(16(13,14)15)3-6(5)8(11)12/h1-3H,(H,9,10)(H,11,12)(H,13,14,15)
| Molecular Formula | C8H6O7S |
| Molecular Weight | 246.194 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| UV-vis absorption properties of polyazomethine in base and protonated with 1,2-(di-2-ethylhexyl)ester of 4-sulfophthalic acid form. | 2009-09-15 |
|
| Preparative separation of isomeric sulfophthalic acids by conventional and pH-zone-refining counter-current chromatography. | 2002-08-09 |
|
| Concerted chemical and microbial degradation of sulfophthalimides formed from sulfophthalocyanine dyes by white-rot fungi. | 2001-12-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:11:18 GMT 2025
by
admin
on
Mon Mar 31 21:11:18 GMT 2025
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| Record UNII |
T1SM5DOM66
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| Record Status |
Validated (UNII)
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| Record Version |
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