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Merck

270865

Sigma-Aldrich

Benzol-1,2-dithiol

96%

Synonym(e):

1,2-Dimercapto-benzol

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About This Item

Lineare Formel:
C6H4(SH)2
CAS-Nummer:
Molekulargewicht:
142.24
Beilstein:
636154
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

96%
96%

Form

liquid

bp

119-120 °C/17 mmHg (lit.)

mp (Schmelzpunkt)

22-24 °C (lit.)

Löslichkeit

water: slightly soluble

Dichte

1.236 g/mL at 25 °C (lit.)

Lagertemp.

2-8°C

SMILES String

Sc1ccccc1S

InChI

1S/C6H6S2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H

InChIKey

JRNVQLOKVMWBFR-UHFFFAOYSA-N

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Allgemeine Beschreibung

The transition metal complexes with benzene-1,2-dithiol as ligand were studied by UV-vis, resonance Raman (rR) and infrared (IR) spectroscopies.

Anwendung

Benzene-1,2-dithiol was used in the preparation of a new type of Schiff base that was required in the synthesis of a new series of copper(II) and zinc(II) complexes.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2

Lagerklassenschlüssel

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flammpunkt (°F)

219.2 °F - closed cup

Flammpunkt (°C)

104 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves


Analysenzertifikate (COA)

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N Raman et al.
European journal of medicinal chemistry, 45(11), 5438-5451 (2010-09-25)
A new series of copper(II) and zinc(II) complexes have been designed and synthesized using a new type of Schiff bases derived from the reaction of 3-(3-phenyl-allylidene)-pentane-2,4-dione with para substituted aniline and benzene-1,2-dithiol. Their structures have been established by analytical and
Lee M, et al.
Royal Society of Chemistry Advances, 5, 86402-86406 (2015)
Taras Petrenko et al.
Journal of the American Chemical Society, 128(13), 4422-4436 (2006-03-30)
Transition metal complexes involving the benzene-1,2-dithiol (L(2-)) and Sellmann's 3,5-di-tert-butylbenzene-1,2-dithiol(L(Bu 2-)) ligands have been studied by UV-vis, infrared (IR), and resonance Raman (rR) spectroscopies. Raman spectra were obtained in resonance with the intervalence charge transfer (IVCT) bands in the near-infrared
Luisa Ugolini et al.
Journal of the science of food and agriculture, 99(9), 4235-4241 (2019-02-26)
The antimicrobial activity of allyl-isothiocyanate (AITC) on plant pathogens is well known and has already been demonstrated in the strawberry with respect to Botritis cinerea fungal infection using postharvest biofumigation. In the present study, vapours of 0.08 mg L-1 of Brassica meal-derived
Mengwei Sun et al.
Molecules (Basel, Switzerland), 24(4) (2019-03-01)
Lung cancer is the leading cause of cancer-related death in the Unites States, and approximately 85% of all lung cancers are classified as non-small cell lung cancer (NSCLC), which is extremely difficult to treat and its survival rate is low.

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