D129208
Toluene-3,4-dithiol
technical grade, 90%
Synonym(s):
3,4-Dimercaptotoluene, 4-Methyl-1,2-benzenedithiol, ‘Dithiol’
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About This Item
Linear Formula:
CH3C6H3(SH)2
CAS Number:
Molecular Weight:
156.27
Beilstein:
1635270
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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grade
technical grade
Quality Level
Assay
90%
form
powder
bp
135-137 °C/17 mmHg (lit.)
mp
30-33 °C (lit.)
density
1.179 g/mL at 25 °C (lit.)
storage temp.
−20°C
SMILES string
Cc1ccc(S)c(S)c1
InChI
1S/C7H8S2/c1-5-2-3-6(8)7(9)4-5/h2-4,8-9H,1H3
InChI key
NIAAGQAEVGMHPM-UHFFFAOYSA-N
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Related Categories
Application
Used to generate the corresponding dithiolate ligand in a study of dinuclear gold(I) dithiolate complexes.[1]
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Inorganic Chemistry, 32, 1749-1749 (1993)
Justin P Bergfield et al.
Nano letters, 11(7), 2759-2764 (2011-06-15)
We investigate electronic transport through molecular radicals and predict a correlation-induced transmission node arising from destructive interference between transport contributions from different charge states of the molecule. This quantum interference effect has no single-particle analog and cannot be described by
Artem Mishchenko et al.
Nano letters, 10(1), 156-163 (2009-12-23)
The conductance of a family of biphenyl-dithiol derivatives with conformationally fixed torsion angle was measured using the scanning tunneling microscopy (STM)-break-junction method. We found that it depends on the torsion angle phi between two phenyl rings; twisting the biphenyl system
Kazunari Yoshizawa
Accounts of chemical research, 45(9), 1612-1621 (2012-06-16)
The transfer of electrons in molecules and solids is an essential process both in biological systems and in electronic devices. Devices that take advantage of the unique electronic properties of a single molecule have attracted much attention, and applications of
Hennie Valkenier et al.
Journal of the American Chemical Society, 133(13), 4930-4939 (2011-03-10)
This Article reports a systematic study on the formation of self-assembled monolayers (SAMs) of conjugated molecules for molecular electronic (ME) devices. We monitored the deprotection reaction of acetyl protected dithiols of oligophenylene ethynylenes (OPEs) in solution using two different bases
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