All Photos(1)
About This Item
Linear Formula:
C10H7CH2CH2OH
CAS Number:
Molecular Weight:
172.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
form
powder
bp
180-184 °C/15 mmHg (lit.)
SMILES string
OCCc1ccc2ccccc2c1
InChI
1S/C12H12O/c13-8-7-10-5-6-11-3-1-2-4-12(11)9-10/h1-6,9,13H,7-8H2
InChI key
VCZANYLMPFRUHG-UHFFFAOYSA-N
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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H Nagaoka et al.
Bioscience, biotechnology, and biochemistry, 63(11), 1991-1992 (2000-01-15)
(S)-1-(2-Naphthyl)ethanol was yielded by immobilized pea (Pisum sativum L.) protein (IPP) from (R, S) 2-naphthyl ethanol (> 99% ee, yield; about 50%), in which the (R)-enantiomer was selectively oxidized to 2-acetonaphthone. IPP could be reused consecutively at least three times
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
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
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
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
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