188107
2-Naphthaleneethanol
98%
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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)
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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)
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
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
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, 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
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