Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H9NO3S |
| Molecular Weight | 223.248 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC=C2C=CC=CC2=C1S(O)(=O)=O
InChI
InChIKey=GWIAAIUASRVOIA-UHFFFAOYSA-N
InChI=1S/C10H9NO3S/c11-9-6-5-7-3-1-2-4-8(7)10(9)15(12,13)14/h1-6H,11H2,(H,12,13,14)
| Molecular Formula | C10H9NO3S |
| Molecular Weight | 223.248 |
| 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 |
|---|---|---|
| Flexible two-dimensional square-grid coordination polymers: structures and functions. | 2010-09-30 |
|
| Reversed-phase liquid chromatographic determination of two manufacturing intermediates in D&C Red No. 34 and its lakes. | 2010-02-20 |
|
| Inclusion complex of 2-naphthylamine-6-sulfonate with beta-cyclodextrin: intramolecular charge transfer versus hydrogen bonding effects. | 2007-04 |
|
| The crystal structure of a cockroach pheromone-binding protein suggests a new ligand binding and release mechanism. | 2003-08-08 |
|
| Inhibition of HIV replication by naphthalenemonosulfonic acid derivatives and a bis naphthalenedisulfonic acid compound. | 1990 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:40:54 GMT 2025
by
admin
on
Mon Mar 31 18:40:54 GMT 2025
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| Record UNII |
F9QKW1FCE0
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID7020922
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81-16-3
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Tobias acid
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C010253
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201-331-5
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m7758
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PRIMARY | Merck Index |