270849
2-Naphthalenethiol
≥95%
Synonym(s):
2-Naphthyl mercaptan, Thio-2-naphthol (β)
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All Photos(2)
About This Item
Linear Formula:
C10H7SH
CAS Number:
Molecular Weight:
160.24
Beilstein/REAXYS Number:
636389
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
≥95%
form
solid
bp
286 °C (lit.)
mp
79-81 °C (lit.)
solubility
diethyl ether: very soluble(lit.)
ethanol: very soluble(lit.)
petroleum ether: very soluble(lit.)
water: slightly soluble(lit.)
SMILES string
Sc1ccc2ccccc2c1
InChI
1S/C10H8S/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H
InChI key
RFCQDOVPMUSZMN-UHFFFAOYSA-N
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General description
The magnetic resonance shift for a self-assembled monolayer of 2-naphthalenethiol was studied that suggested considerable promise in flexible and transparent photonic devices for biological and chemical sensing.
Application
2-Naphthalenethiol was used in the preparation of cholesterol monolayer and multilayer Langmuir- Blodgett (LB) films. The electrochemical barrier properties of these films were studied using cyclic voltammetry and electrochemical impedance spectroscopy.
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Xinlong Xu et al.
Nano letters, 11(8), 3232-3238 (2011-06-24)
Flexible electronic and photonic devices have been demonstrated in the past decade, with significant promise in low-cost, light-weighted, transparent, biocompatible, and portable devices for a wide range of applications. Herein, we demonstrate a flexible metamaterial (Metaflex)-based photonic device operating in
A bioinspired approach for controlling accessibility in calix[4]arene-bound metal cluster catalysts.
Namal de Silva et al.
Nature chemistry, 2(12), 1062-1068 (2010-11-26)
In enzymes, the electronic and steric environments of active centres, and therefore their activity in biological processes, are controlled by the surrounding amino acids. In a similar manner, organic ligands have been used for the 'passivation' of metal clusters, that
Metal-cluster catalysts: Access granted.
Graham J Hutchings
Nature chemistry, 2(12), 1005-1006 (2010-11-26)
J Ni et al.
Analytical chemistry, 71(21), 4903-4908 (1999-11-24)
An immunoassay readout method based on surface-enhanced Raman scattering (SERS) is described. The method exploits the SERS-derived signal from reporter molecules that are coimmobilized with biospecific species on gold colloids. This concept is demonstrated in a dualanalyte sandwich assay, in
Peng Jiang et al.
Journal of the American Chemical Society, 128(38), 12390-12391 (2006-09-21)
We evidence by STM that 2-naphthalenethiol self-assembled monolayers formed at the n-tetradecane/Au(111) interface coexist as two structural phases which both possess molecules into two different orientations (standing and lying). Such a rotational polymorphism is observed and understood at the molecular
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