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Details

Stereochemistry ACHIRAL
Molecular Formula C12H10O3
Molecular Weight 202.206
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6-METHOXY-2-NAPHTHOIC ACID

SMILES

COC1=CC2=CC=C(C=C2C=C1)C(O)=O

InChI

InChIKey=YZBILXXOZFORFE-UHFFFAOYSA-N
InChI=1S/C12H10O3/c1-15-11-5-4-8-6-10(12(13)14)3-2-9(8)7-11/h2-7H,1H3,(H,13,14)

HIDE SMILES / InChI

Molecular Formula C12H10O3
Molecular Weight 202.206
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis of some new 2-(6-methoxy-2-naphthyl)- 5-aryl-1,3,4-oxadiazoles as possible non-steroidal anti-inflammatory and analgesic agents.
2005 Aug
Design, synthesis and evaluation of naphthalene-2-carboxamides as reversal agents in MDR cancer.
2006 Sep 1
Patents
Substance Class Chemical
Created
by admin
on Tue Oct 22 13:56:24 UTC 2019
Edited
by admin
on Tue Oct 22 13:56:24 UTC 2019
Record UNII
65IH1SV66A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
6-METHOXY-2-NAPHTHOIC ACID
Systematic Name English
2-NAPHTHALENECARBOXYLIC ACID, 6-METHOXY-
Systematic Name English
6-METHOXY-2-NAPHTHALENECARBOXYLIC ACID
Systematic Name English
NAPROXEN RELATED COMPOUND A [USP-RS]
Common Name English
2-METHOXY-6-NAPHTHALENECARBOXYLIC ACID
Systematic Name English
NAPROXEN RELATED COMPOUND A
USP-RS  
Common Name English
NAPROXEN SPECIFIED IMPURITY O [EP]
Common Name English
NSC-408786
Code English
Code System Code Type Description
PUBCHEM
349181
Created by admin on Tue Oct 22 13:56:24 UTC 2019 , Edited by admin on Tue Oct 22 13:56:24 UTC 2019
PRIMARY
EPA CompTox
2471-70-7
Created by admin on Tue Oct 22 13:56:24 UTC 2019 , Edited by admin on Tue Oct 22 13:56:24 UTC 2019
PRIMARY
CAS
2471-70-7
Created by admin on Tue Oct 22 13:56:24 UTC 2019 , Edited by admin on Tue Oct 22 13:56:24 UTC 2019
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
For the calculation of contents, multiply the peak areas by 2.0
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP