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58468-22-7

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58468-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58468-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,6 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58468-22:
(7*5)+(6*8)+(5*4)+(4*6)+(3*8)+(2*2)+(1*2)=157
157 % 10 = 7
So 58468-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H18S6/c1-13-7-8(14-2)10(16-4)12(18-6)11(17-5)9(7)15-3/h1-6H3

58468-22-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5,6-hexakis(methylsulfanyl)benzene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58468-22-7 SDS

58468-22-7Relevant articles and documents

Donor-substituted CpCo-stabilized cyclobutadienes and superphanes

Werz, Daniel B.,Schulte, J. Hilko,Gleiter, Rolf,Rominger, Frank

, p. 3132 - 3142 (2004)

RCpCoL2 complexes (L2 = (CO)2 or COD, R = H, CO2Me, TMS) were reacted with various alkynes substituted with chalcogen atoms adjacent to the triple bonds. These reactions yielded hetero-substituted CpCo-capped cyclobutadienes and superphanes dependent on the ring size of the corresponding cyclic diene used as starting material. Reactions in decaline afforded not only CpCo-capped cyclobutadieno superphanes, but also mixed cyclobutadieno cyclopentadienono superphanes. X-ray analyses do not indicate a significant amount of conjugation between the π systems and the lone pairs of the heteroatoms whereas cyclic voltammetry reveals an easier oxidation when increasing the number of electron-donating heteroatoms.

Highly Conductive 2D Metal-Organic Framework Thin Film Fabricated by Liquid-Liquid Interfacial Reaction Using One-Pot-Synthesized Benzenehexathiol

Chen, Iu-Fan,Lu, Chun-Fu,Su, Wei-Fang

, p. 15754 - 15762 (2019/01/09)

Metal-organic frameworks (MOF) are studied extensively in applications like catalysts, gas storage, and sensors due to their various functional groups and structures. Two-dimensional (2D) MOFs such as triphenylene-based materials show excellent charge transport properties, but thin-film fabrication and organic ligand synthesis are difficult. In this work, we synthesize thiol-based organic ligand, benzenehexathiol (BHT), by a simple one-pot reaction. This facile method is safer and faster than conventional synthesis procedure that requires using liquid ammonia as solvent. Two novel 2D MOF materials, Ag3BHT2 and Au3BHT2, are fabricated by coordinating BHT with either silver (Ag) or gold (Au) ions through liquid-liquid interfacial reaction. The Ag3BHT2 thin film reaches a high electrical conductivity of 363 S cm-1, which has potential applications in electronic devices and sensors.

AN ELECTRON SPIN RESONANCE INVESTIGATION OF THE RADICAL CATIONS FROM POLY(ALKYLTHIO)BENZENES

Alberti, Angelo,Pedulli, Gian Franco,Tiecco, Marcello,Testaferri, Lorenzo,Tingoli, Marco

, p. 975 - 980 (2007/10/02)

The radical cations of some poly(methylthio)- and poly(isopropylthio)-benzenes have been investigated by e.s.r. spectroscopy.Discrimination between the couplings due to the aryl and alkyl protons, when the assignment is not straightforward, has been made

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