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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
Structure of 2-NAPHTHYLAMINE-1-SULFONIC ACID

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)

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Inhibition of HIV replication by naphthalenemonosulfonic acid derivatives and a bis naphthalenedisulfonic acid compound.
1990
The crystal structure of a cockroach pheromone-binding protein suggests a new ligand binding and release mechanism.
2003 Aug 8
Inclusion complex of 2-naphthylamine-6-sulfonate with beta-cyclodextrin: intramolecular charge transfer versus hydrogen bonding effects.
2007 Apr
Reversed-phase liquid chromatographic determination of two manufacturing intermediates in D&C Red No. 34 and its lakes.
2009 Nov-Dec
Flexible two-dimensional square-grid coordination polymers: structures and functions.
2010 Sep 30
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:08:57 GMT 2023
Edited
by admin
on Fri Dec 15 17:08:57 GMT 2023
Record UNII
F9QKW1FCE0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-NAPHTHYLAMINE-1-SULFONIC ACID
MI  
Common Name English
1-NAPHTHALENESULFONIC ACID, 2-AMINO-
Common Name English
TOBIAS ACID
Common Name English
2-AMINO-1-NAPHTHALENESULFONIC ACID
HSDB  
Systematic Name English
AMINO-1-NAPHTHALENESULFONIC ACID, 2-
Common Name English
2-NAPHTHYLAMINE-1-SULFONIC ACID [MI]
Common Name English
NSC-5523
Code English
2-AMINO-1-NAPHTHALENESULFONIC ACID [HSDB]
Common Name English
Code System Code Type Description
FDA UNII
F9QKW1FCE0
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY
EPA CompTox
DTXSID7020922
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY
PUBCHEM
6670
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY
HSDB
5239
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY
CAS
81-16-3
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY
WIKIPEDIA
Tobias acid
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY
MESH
C010253
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY
NSC
5523
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-331-5
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY
MERCK INDEX
m7758
Created by admin on Fri Dec 15 17:08:57 GMT 2023 , Edited by admin on Fri Dec 15 17:08:57 GMT 2023
PRIMARY Merck Index