270849
2-Naphthalenethiol
≥95%
Synonym(s):
2-Naphthyl mercaptan, Thio-2-naphthol (β)
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About This Item
Linear Formula:
C10H7SH
CAS Number:
Molecular Weight:
160.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-082-5
Beilstein/REAXYS Number:
636389
MDL number:
Product Name
2-Naphthalenethiol, ≥95%
InChI key
RFCQDOVPMUSZMN-UHFFFAOYSA-N
InChI
1S/C10H8S/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H
SMILES string
Sc1ccc2ccccc2c1
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.)
Quality Level
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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.
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.
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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
Metal-cluster catalysts: Access granted.
Graham J Hutchings
Nature chemistry, 2(12), 1005-1006 (2010-11-26)
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
Surface-enhanced Raman scattering for ultrasensitive chemical analysis of 1 and 2-naphthalenethiols.
R A Alvarez-Puebla et al.
The Analyst, 129(12), 1251-1256 (2004-11-27)
The results of the search for the optimal experimental conditions for ultrasentitive chemical analysis of 1-naphthalenethiol (1-NAT) and 2-naphthalenethiol (2-NAT) using surface-enhanced Raman scattering (SERS) are discussed. The report begins with a review of the vibrational spectra, including infrared and
Rakesh K Pandey et al.
Journal of colloid and interface science, 315(2), 528-536 (2007-08-19)
We have formed the cholesterol monolayer and multilayer LB films on the self-assembled monolayers of 2-naphthalenethiol (2-NT) and thiophenol (TP) and studied the electrochemical barrier properties of these composite films using cyclic voltammetry and electrochemical impedance spectroscopy. We have also
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