3,4-toluenedithiol
3,4-toluenedithiol structure
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Common Name | 3,4-toluenedithiol | ||
|---|---|---|---|---|
| CAS Number | 496-74-2 | Molecular Weight | 156.268 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 265.5±20.0 °C at 760 mmHg | |
| Molecular Formula | C7H8S2 | Melting Point | 30-33 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 122.8±15.7 °C | |
| Symbol |
GHS05, GHS07 |
Signal Word | Danger | |
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Determination of residual arsenic compounds in chicken muscle by ultra-performance liquid chromatography coupled with ultraviolet detection after pre-column derivatization with toluene-3,4-dithiol.
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 1006 , 151-7, (2015) A simple and sensitive derivatization method using toluene-3,4-dithiol as a derivatization reagent for the simultaneous analysis of seven arsenic compounds (roxarsone, nitarsone, p-arsanilic acid, o-arsanilic acid, phenylarsonic acid, phenylarsine oxide, and ... |
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Epidithiol formation by an unprecedented twin carbon-sulfur lyase in the gliotoxin pathway.
Angew. Chem. Int. Ed. Engl. 51(40) , 10064-8, (2012)
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Chelate-Thiolate-Coordinate Ligands Modulating the Configuration and Electrochemical Property of Dinitrosyliron Complexes (DNICs).
Chemistry 21 , 16035-46, (2015) As opposed to the reversible redox reaction ({Fe(NO)2 }(10) reduced-form DNIC [(NO)2 Fe(S(CH2 )3 S)](2-) (1)⇌{Fe(NO)2 }(9) oxidized-form [(NO)2 Fe(S(CH2 )3 S)](-) ), the chemical oxidation of the {Fe(NO)2 }(10) DNIC [(NO)2 Fe(S(CH2 )2 S)](2-) (2) generates th... |
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Synthesis and characterization of toluene-3,4-dithiolatoantimony(III) derivatives with some oxygen and/or sulphur donor ligands.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 74(1) , 67-73, (2009) Replacement reactions of toluene-3,4-dithiolatoantimony(III) chloride with oxygen and/or sulphur donor ligands like benzoic acid, thiobenzoic acid, thioacetic acid, phenol, thiophenol, sodium salicylate and thio glycolic acid in 1:1 molar ratio as well as dis... |
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An Inhibitory Antibody Blocks the First Step in the Dithiol/Disulfide Relay Mechanism of the Enzyme QSOX1
J. Mol. Biol. 425(22) , 4366-78, (2013) Quiescin sulfhydryl oxidase 1 (QSOX1) is a catalyst of disulfide bond formation that undergoes regulated secretion from fibroblasts and is over-produced in adenocarcinomas and other cancers. We have recently shown that QSOX1 is required for incorporation of p... |
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Glutathione regulates the transfer of iron-sulfur cluster from monothiol and dithiol glutaredoxins to apo ferredoxin.
Protein Cell. 3(9) , 714-21, (2012) Holo glutaredoxin (Grx) is a homo-dimer that bridges a [2Fe-2S] cluster with two glutathione (GSH) ligands. In this study, both monothiol and dithiol holo Grxs are found capable of transferring their iron-sulfur (FeS) cluster to an apo ferredoxin (Fdx) throug... |
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3-(2-aminophenyl)-4-methyl-1,3-thiazole-2(3H)-thione as an ecofriendly sulphur transfer agent to prepare alkanethiols in high yield and high purity.
Molecules 14(11) , 4634-43, (2009) A new process is described for preparing very pure linear alkanethiols and linear alpha,omega-alkanedithiols using a sequential alkylation of the title compound, followed by a ring closure to quantitatively give the corresponding 3-methyl[1,3]thiazolo[3,2-a]-... |
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An orbital rule for electron transport in molecules.
Acc. Chem. Res. 45(9) , 1612-21, (2012) 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 application... |
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Synthesis of sulfuric macrocycles and a rotaxane through thiol-yne click and dithiol coupling reactions.
Org. Lett. 12(18) , 4078-81, (2010) 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 thro... |
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Insights into the specificity of thioredoxin reductase-thioredoxin interactions. A structural and functional investigation of the yeast thioredoxin system.
Biochemistry 49(15) , 3317-26, (2010) The enzymatic activity of thioredoxin reductase enzymes is endowed by at least two redox centers: a flavin and a dithiol/disulfide CXXC motif. The interaction between thioredoxin reductase and thioredoxin is generally species-specific, but the molecular aspec... |