188107
2-Naphthaleneethanol
98%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
C10H7CH2CH2OH
CAS Number:
Molecular Weight:
172.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
216-061-3
MDL number:
Assay:
98%
Form:
powder
assay
98%
form
powder
InChI key
VCZANYLMPFRUHG-UHFFFAOYSA-N
InChI
1S/C12H12O/c13-8-7-10-5-6-11-3-1-2-4-12(11)9-10/h1-6,9,13H,7-8H2
SMILES string
OCCc1ccc2ccccc2c1
bp
180-184 °C/15 mmHg (lit.)
functional group
hydroxyl
Gene Information
human ... BAD(572)
General description
2-Naphthaleneethanol undergoes esterification reaction with poly(ethylene glycol) monomethyl ether carboxylic acid. Emission spectra of 2-naphthaleneethanol reacted with UV-irradiated octadecylsiloxane self-assembled monolayers has been investigated.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
V Schurig et al.
Journal of biochemical and biophysical methods, 43(1-3), 223-240 (2000-06-28)
The use of complexation SFC for enantiomer separation of Lewis base selectands on chiral nickel(II)- and zinc(II)-bis[(3-heptafluorobutanoyl)-10-methylene-(1R)-camphora te] chemically bonded to poly(dimethylsiloxane) (Chirasil-nickel and Chirasil-zinc) and employed as Lewis acid selectors is described. The method is especially suited for less
H Nagaoka et al.
Bioscience, biotechnology, and biochemistry, 64(4), 781-784 (2000-06-01)
Kinetic resolution of racemic alcohols, (+/-)-1-(4-substituted phenyl)ethanol and (+/-)-1-(2-naphthyl)ethanol, was done with immobilized green pea, soybean, or buckwheat proteins. The resolution was done stereoselectively by oxidizing only one enantiomer of a racemic alcohol to leave an optically active alcohol with
Alkoxyacetyl (AAc) group as a useful linker for organic synthesis on poly (ethylene glycol) support.
Oikawa M, et al.
Tetrahedron Letters, 45(11), 2371-2375 (2004)
Eric A McArthur et al.
Journal of the American Chemical Society, 126(8), 2260-2261 (2004-02-26)
Detection and quantification of submonolayer coverage surface species is not trivial. We have developed a novel method sensitive to surface-bound chemical functional groups as low as 10(11) molecules/cm(2) by specific covalent attachment of fluorescent chromophores. This enables the intermediates of
N Seurre et al.
Physical chemistry chemical physics : PCCP, 8(8), 1007-1016 (2006-02-17)
Jet-cooled diastereoisomeric complexes formed between a chiral probe, (+/-)-2-naphthyl-1-ethanol, and chiral lactic acid derivatives have been characterised by laser-induced fluorescence and IR fluorescence-dip spectroscopy. Complexes with non chiral alpha-hydroxyesters and chiral beta-hydroxyesters have also been studied for the sake of
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service