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Details

Stereochemistry ACHIRAL
Molecular Formula C10H8S
Molecular Weight 160.236
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-NAPHTHALENETHIOL

SMILES

SC1=CC=C2C=CC=CC2=C1

InChI

InChIKey=RFCQDOVPMUSZMN-UHFFFAOYSA-N
InChI=1S/C10H8S/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H

HIDE SMILES / InChI

Molecular Formula C10H8S
Molecular Weight 160.236
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Surface-enhanced Raman scattering for ultrasensitive chemical analysis of 1 and 2-naphthalenethiols.
2004 Dec
Activation of the sulfhydryl group by Mo centers: kinetics of reaction of benzyl radical with a binuclear Mo(micro-SH)Mo complex and with arene and alkane thiols.
2004 Jun 2
Exploring the boundaries of a light-driven molecular motor design: new sterically overcrowded alkenes with preferred direction of rotation.
2004 May 21
Surface-enhanced raman scattering on dendrimer/metallic nanoparticle layer-by-layer film substrates.
2005 Jun 7
Role of nanoparticle surface charge in surface-enhanced Raman scattering.
2005 Mar 10
Scanning tunneling microscopy, Fourier transform infrared spectroscopy, and electrochemical characterization of 2-naphthalenethiol self-assembled monolayers on the Au surface: a study of bridge-mediated electron transfer in Ru(NH3)6(2+)/Ru(NH3)6(3+) redox reactions.
2005 Sep 1
Structural changes in self-assembled monolayers initiated by ultraviolet light.
2006 Aug 17
Rotational polymorphism in 2-naphthalenethiol SAMs on Au(111).
2006 Sep 27
Surface-enhanced Raman spectroscopic-encoded beads for multiplex immunoassay.
2007 Mar-Apr
Electron transfer studies on cholesterol LB films assembled on thiophenol and 2-naphthalenethiol self-assembled monolayers.
2007 Nov 15
Silica-void-gold nanoparticles: temporally stable surface-enhanced Raman scattering substrates.
2008 Oct 29
Quantitative structure-activity relationship study on the anti-HIV-1 activity of novel 6-naphthylthio HEPT analogs.
2009 Aug
Protein separation and identification using magnetic beads encoded with surface-enhanced Raman spectroscopy.
2009 Aug 1
A multi-technique approach to the analysis of SAMs of aromatic thiols on copper.
2009 Dec 28
Friction of polyaromatic thiol monolayers in adhesive and nonadhesive contacts.
2009 Oct 20
Encapsulation of zinc oxide nanorods and nanoparticles.
2009 Sep 1
Synthesis and characterization of accessible metal surfaces in calixarene-bound gold nanoparticles.
2009 Sep 15
Application of nanomaterials in two-terminal resistive-switching memory devices.
2010
Copper protection by self-assembled monolayers of aromatic thiols in alkaline solutions.
2010 Aug 28
A bioinspired approach for controlling accessibility in calix[4]arene-bound metal cluster catalysts.
2010 Dec
Selective inhibitors of the JMJD2 histone demethylases: combined nondenaturing mass spectrometric screening and crystallographic approaches.
2010 Feb 25
SERS decoding of micro gold shells moving in microfluidic systems.
2010 May
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:14:58 GMT 2023
Edited
by admin
on Fri Dec 15 19:14:58 GMT 2023
Record UNII
SZ5U1S741V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-NAPHTHALENETHIOL
MI  
Systematic Name English
.BETA.-NAPHTHALENETHIOL
Systematic Name English
2-MERCAPTONAPHTHALENE
Systematic Name English
2-NAPHTHALENETHIOL [MI]
Common Name English
.BETA.-NAPHTHYL MERCAPTAN
Systematic Name English
2-THIONAPHTHOL
Common Name English
.BETA.-THIONAPHTHOL
Common Name English
VULCAMEL TBN
Common Name English
2-NAPHTHYL MERCAPTAN
FHFI  
Systematic Name English
FEMA NO. 3314
Code English
2-NAPHTHYL MERCAPTAN [FHFI]
Common Name English
NSC-4749
Code English
.BETA.-MERCAPTONAPHTHALENE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 2-NAPHTHALENETHIOL
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
Code System Code Type Description
PUBCHEM
7058
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY
CAS
91-60-1
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY
WIKIPEDIA
2-Naphthalenethiol
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY
MERCK INDEX
m7734
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY Merck Index
MESH
C401958
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY
FDA UNII
SZ5U1S741V
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY
NSC
4749
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY
JECFA MONOGRAPH
681
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-082-5
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID1059028
Created by admin on Fri Dec 15 19:14:58 GMT 2023 , Edited by admin on Fri Dec 15 19:14:58 GMT 2023
PRIMARY