70660
2-Naphthoxyacetic acid
technical, ≥90% (T)
Sinônimo(s):
BNOA
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About This Item
Fórmula linear:
C10H7OCH2CO2H
Número CAS:
Peso molecular:
202.21
Beilstein:
1074148
Número CE:
Número MDL:
Código UNSPSC:
12352100
Produtos recomendados
grau
technical
Ensaio
≥90% (T)
pf
151-154 °C (lit.)
151-154 °C
cadeia de caracteres SMILES
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)
chave InChI
RZCJYMOBWVJQGV-UHFFFAOYSA-N
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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
L Li et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(8), 1513-1521 (2000-07-25)
A cyclodextrin induced room temperature phosphorimetry (CD-RTP) for determine beta-NOA, which using I- as a heavy atom perturber (HAP) and sodium sulfite as a deoxygenator, was developed. The phosphorescence peak wavelength maxima lambda(ex)/lambda(em) = 287/496,521 nm. The analytical curve of
Chun Zhou et al.
Environmental monitoring and assessment, 154(1-4), 233-239 (2008-06-17)
A reliable and sensitive competitive fluorescence immunoassay for the quantitative determination of naphthalene (NA) was developed. 2-naphthoxy acetic acid (NAA) was selected as the hapten of naphthalene. Active ester method (AEM) was used to couple the NAA to carrier proteins
Tsai-Hui Duh et al.
Journal of chromatography. A, 987(1-2), 205-209 (2003-03-05)
In continuing the search for fluorescent reagents for analytical derivatization in chromatography, we found a simple chemical, (2-naphthoxy)acetyl chloride, with potential fluorophore/chromophore characteristics for the highly sensitive detection of analytes with an amino function. The reagent has an auxochrome (a
Sanghamitra Atta et al.
Journal of photochemistry and photobiology. B, Biology, 111, 39-49 (2012-04-20)
We report a novel technique for controlled release of plant growth regulators (PGRs) by sunlight using photoremovable protecting group (PRPG) as a delivery device. In the present work, carboxyl-containing PGRs of the auxin group [indoleacetic acid (IAA) and naphthoxyacetic acid
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