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Merck

N3405

2-Naphthoxyacetic acid

98%

Synonym(s):

BNOA

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About This Item

Linear Formula:
C10H7OCH2CO2H
CAS Number:
Molecular Weight:
202.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-380-0
Beilstein/REAXYS Number:
1074148
MDL number:
Assay:
98%
Form:
powder
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Quality Level

assay

98%

form

powder

mp

151-154 °C (lit.)

SMILES string

OC(=O)COc1ccc2ccccc2c1

InChI

1S/C12H10O3/c13-12(14)8-15-11-6-5-9-3-1-2-4-10(9)7-11/h1-7H,8H2,(H,13,14)

InChI key

RZCJYMOBWVJQGV-UHFFFAOYSA-N

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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M Illangasekare et al.
Science (New York, N.Y.), 267(5198), 643-647 (1995-02-03)
An RNA has been selected that rapidly aminoacylates its 2'(3') terminus when provided with phenylalanyl-adenosine monophosphate. That is, the RNA accelerates the same aminoacyl group transfer catalyzed by protein aminoacyl-transfer RNA synthetases. The best characterized RNA reaction requires both Mg2+
Asuman Karadeniz et al.
Toxicology and industrial health, 27(9), 840-848 (2011-04-23)
In this study, the mutagenic and recombinogenic effects of indole-3-acetic acid (IAA), a plant growth regulator naturally synthesized in plants but produced synthetically, and β-naphthoxyacetic acid (BNOA), a synthetic plant growth regulator widely used in agricultural regions, were investigated using
Poonam Piplani et al.
Medicinal chemistry (Shariqah (United Arab Emirates)), 9(3), 371-378 (2012-08-28)
The present paper describes the design and synthesis of a series of some 2-naphthyloxy derivatives with their antiamnesic activity using mice as the animal model and piracetam as the reference drug. All the synthesized compounds were characterized by spectroscopic techniques
D Hössel et al.
Plant biology (Stuttgart, Germany), 7(1), 41-48 (2005-01-25)
A study of transport and action of synthetic auxin analogues can help to identify transporters and receptors of this plant hormone. Both aspects--transportability and action on growth--were tested with 2-naphthoxyacetic acid (2-NOA) and compared across several plant species. 2-NOA stimulates
A Kokkinou et al.
Carbohydrate research, 332(1), 85-94 (2001-06-14)
The structure of the complex of beta-cyclodextrin (cyclomaltoheptaose) with beta-naphthyloxyacetic acid was studied in solid state by X-ray diffraction and in aqueous solution by 1H NMR spectroscopy. The complex crystallizes in the channel mode, space group C2, with a stoichiometry

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