270849
2-Naphthalenethiol
≥95%
Sinónimos:
2-Naphthyl mercaptan, Thio-2-naphthol (β)
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Fórmula lineal:
C10H7SH
Número CAS:
Peso molecular:
160.24
Beilstein/REAXYS Number:
636389
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Permítanos ayudarleQuality 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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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
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Graham J Hutchings
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Namal de Silva et al.
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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
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
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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