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Merck
CN

W331401

Sigma-Aldrich

2-Naphthalenethiol

99%

Synonym(s):

2-Naphthyl mercaptan, Thio-2-naphthol (β)

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About This Item

Linear Formula:
C10H7SH
CAS Number:
91-60-1
Molecular Weight:
160.24
FEMA Number:
3314
Beilstein:
636389
EC Number:
202-082-5
MDL number:
MFCD00004086
UNSPSC Code:
12164502
PubChem Substance ID:
329830596
Flavis number:
12.033

Key Documents

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biological source

synthetic

Assay

99%

bp

286 °C (lit.)

mp

79-81 °C (lit.)

application(s)

flavors and fragrances

Organoleptic

sulfurous

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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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKBG8736V
14931AE

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Metal-cluster catalysts: Access granted.
Graham J Hutchings
Nature chemistry, 2(12), 1005-1006 (2010-11-26)
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
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
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
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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