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Details

Stereochemistry ACHIRAL
Molecular Formula C12H10O2
Molecular Weight 186.2066
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-NAPHTHALENEACETIC ACID

SMILES

OC(=O)CC1=CC=C2C=CC=CC2=C1

InChI

InChIKey=VIBOGIYPPWLDTI-UHFFFAOYSA-N
InChI=1S/C12H10O2/c13-12(14)8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2,(H,13,14)

HIDE SMILES / InChI

Molecular Formula C12H10O2
Molecular Weight 186.2066
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Auxin influx inhibitors 1-NOA, 2-NOA, and CHPAA interfere with membrane dynamics in tobacco cells.
2010-08
Activity of increased specific and non-specific esterases and glutathione transferases associated with resistance to permethrin in pediculus humanus capitis (phthiraptera: pediculidae) from Argentina.
2010-01
[Genotypical peculiarities of expression of the beta-specific carboxylic ester hydrolase allozymes in Drosophila melanogaster of wild type].
2009-03-04
Structure and photochemical properties of (mu-alkoxo)bis(mu-carboxylato)diruthenium complexes with naphthylacetate ligands.
2006-04-03
Site-specific carbon isotope analysis of aromatic carboxylic acids by elemental analysis/pyrolysis/isotope ratio mass spectrometry.
2006
Butyrylcholinesterase, paraoxonase, and albumin esterase, but not carboxylesterase, are present in human plasma.
2005-11-25
The Arabidopsis F-box protein TIR1 is an auxin receptor.
2005-05-26
[Growth-regulating activity of N-benzyl- and O-benzyl-containing compounds belonging to a new group of synthetic analogues of natural auxins].
2005-04-30
The functional role of threonine-205 in the mechanism-based inactivation of P450 2B1 by two ethynyl substrates: the importance of the F helix in catalysis.
2004-12
Effect of the addition of a nonaqueous polar solvent (glycerol) on enzymatic catalysis in reverse micelles. Hydrolysis of 2-naphthyl acetate by alpha-chymotrypsin.
2004-07-06
Remarkably enhanced excimer formation of naphthylacetate in cation-charged gamma-cyclodextrin.
2003-05-15
Feasibility of atmospheric pressure desorption/ionization on silicon mass spectrometry in analysis of drugs.
2003
Identification and quantification of polar naphthalene derivatives in contaminated groundwater of a former gas plant site by liquid chromatography-electrospray ionization tandem mass spectrometry.
2002-08-23
Esterase isozyme polymorphism, specific and nonspecific esterase, syngenic lines development and natural occurrence of a thermostable esterase in the tropical silkworm Bombyx mori L.
2001-11-01
A procedure for the joint evaluation of substrate partitioning and kinetic parameters for reactions catalyzed by enzymes in reverse micellar solutions. I. Hydrolysis of 2-naphthyl acetate catalyzed by lipase in sodium 1,4-bis(2-ethylhexyl) sulphosuccinate (AOT)/buffer/heptane.
2001-04-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:34:42 GMT 2025
Edited
by admin
on Mon Mar 31 19:34:42 GMT 2025
Record UNII
202H99Z0CE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-NAPHTHALENEACETIC ACID
Systematic Name English
NSC-301
Preferred Name English
2-NAPHTHYLACETIC ACID
Systematic Name English
2-(2-NAPHTHYL)ACETIC ACID
Systematic Name English
2-NAPHTHALEN-2-YLACETIC ACID
Systematic Name English
.BETA.-NAPHTHALENEACETATE
Systematic Name English
BETOXAN
Common Name English
NAPHTHYLACETIC ACID, 2-
Common Name English
.BETA.-NAPHTHYLACETIC ACID
Systematic Name English
NAPHTHALEN-2-YLACETIC ACID
Systematic Name English
.BETA.-NAPHTHALENEACETIC ACID
Systematic Name English
Code System Code Type Description
FDA UNII
202H99Z0CE
Created by admin on Mon Mar 31 19:34:42 GMT 2025 , Edited by admin on Mon Mar 31 19:34:42 GMT 2025
PRIMARY
CHEBI
37837
Created by admin on Mon Mar 31 19:34:42 GMT 2025 , Edited by admin on Mon Mar 31 19:34:42 GMT 2025
PRIMARY
CAS
581-96-4
Created by admin on Mon Mar 31 19:34:42 GMT 2025 , Edited by admin on Mon Mar 31 19:34:42 GMT 2025
PRIMARY
PUBCHEM
11393
Created by admin on Mon Mar 31 19:34:42 GMT 2025 , Edited by admin on Mon Mar 31 19:34:42 GMT 2025
PRIMARY
NSC
301
Created by admin on Mon Mar 31 19:34:42 GMT 2025 , Edited by admin on Mon Mar 31 19:34:42 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-475-0
Created by admin on Mon Mar 31 19:34:42 GMT 2025 , Edited by admin on Mon Mar 31 19:34:42 GMT 2025
PRIMARY
EPA CompTox
DTXSID20206825
Created by admin on Mon Mar 31 19:34:42 GMT 2025 , Edited by admin on Mon Mar 31 19:34:42 GMT 2025
PRIMARY