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 active site of the [FeFe] hydrogenases contains two Fe ions bound to one Cys ligand, three CO molecules, two CN(-) ions, and a dithiolate ligand. The nature of the last of these has been much discussed, and it has
Weidong Zhou et al.
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A macrocycle and a rotaxane were constructed by virtue of the thiol-yne click reaction under the irradiation of light in high yield, which can proceed at ambient temperature and humidity under an air atmosphere. Two disulfide macrocycles were synthesized through
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The reaction of [Ru(III)(cyclam)Cl(2)]Cl with 2 equiv of sodium N,N-diethyldithiocarbamate in methanol afforded [Ru(II)(cyclam)(Et(2)dtc)](BPh(4)) (1(BPh(4))). The same reaction with only 1 equiv of toluene-3,4-dithiol and a base yielded [Ru(cyclam)(tdt)](PF(6)) (2(PF(6))) which was oxidized by 1 equiv of ferrocenium hexafluorophosphate generating
A stable acyclic ligand equivalent of an unstable 1,3-dithiol-5-ylidene.
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