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
Recommended Products
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.
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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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
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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
Kazunari Yoshizawa
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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
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