760080
4′-Mercaptobiphenylcarbonitrile
97% (GC)
Synonym(s):
4′-Mercapto-[1,1′-biphenyl]-4-carbonitrile
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About This Item
Empirical Formula (Hill Notation):
C13H9NS
CAS Number:
Molecular Weight:
211.28
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23
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Quality Level
assay
97% (GC)
form
powder
mp
127-132 °C
SMILES string
Sc1ccc(cc1)-c2ccc(cc2)C#N
InChI
1S/C13H9NS/c14-9-10-1-3-11(4-2-10)12-5-7-13(15)8-6-12/h1-8,15H
InChI key
ZZSHJNKMDIZSFY-UHFFFAOYSA-N
Related Categories
Application
This material is used to tune the electronic properties and subsequent surface coverage of gold surfaces/monolayer.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Nikolaus Meyerbröker et al.
Langmuir : the ACS journal of surfaces and colloids, 28(25), 9583-9592 (2012-06-02)
Here we describe the behavior of self-assembled monolayers (SAMs) of 4'-cyanobiphenyl-4-thiol (CBPT) on Au(111) upon electron irradiation. Under such a treatment, the aromatic framework of CBPT SAMs is laterally cross-linked while the nitrile groups, located at the SAM-ambience interface, are
Ferdinand Rissner et al.
ACS nano, 4(11), 6735-6746 (2010-11-05)
The electronic structure of mixed self-assembled monolayers (SAMs) on Au(111) surfaces is modeled using slab-type density-functional theory calculations. The studied molecules have a dipolar character induced by polar and electron donating or accepting tail-group substituents. The resulting electronic structure of
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