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24455-28-5

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24455-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24455-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,5 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24455-28:
(7*2)+(6*4)+(5*4)+(4*5)+(3*5)+(2*2)+(1*8)=105
105 % 10 = 5
So 24455-28-5 is a valid CAS Registry Number.

24455-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis[(4-methylphenyl)sulfanyl]methanethione

1.2 Other means of identification

Product number -
Other names trithiocarbonic acid di-p-tolyl ester

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:24455-28-5 SDS

24455-28-5Relevant articles and documents

Synthesis and characterization of magnetic copper ferrite nanoparticles and their catalytic performance in one-pot odorless carbon-sulfur bond formation reactions

Gholinejad, Mohammad,Karimi, Babak,Mansouri, Fariborz

, p. 20 - 27 (2014/03/21)

In this article, we have introduced catalytic application of copper ferrite nanoparticles (CuFe2O4) for one-pot odorless production of aryl alkyl thioethers using thiourea and alkyl bromides in wet polyethylene glycol as a green solvent. The catalyst was also successfully applied for one-pot synthesis of symmetrical diaryl trithiocarbonates via the reaction of sodium sulfide, carbon disulfide and aryl iodides under heterogeneous reaction condition. Magnetic copper ferrite nanoparticles were synthesized using iron (III) chloride and copper (II) chloride, and characterized using XRD, FT-IR, AAS, and TEM analysis. The catalyst was recycled using simple magnetic separation and reused for the five consecutive runs in the reaction of iodobenzene, thiourea and benzyl bromide without appreciable loss of activity.

SYNTHESIS, STRUCTURE, AND REACTIONS OF THIOCARBONIC ACID DERIVATIVES NEW PENTATHIODIPERCARBONATES, (RSS)2C=S, α,α,α-TRIS(DISULFIDES), AND THE FIRST α,α,α-TRIS(TRISULFIDE)

Hansen, Holger C.,Senning, Alexander,Hazell, Rita G.

, p. 5145 - 5158 (2007/10/02)

Novel bis(perhaloalkyl) pentathiodipercarbonates 5b-d have been synthesised by reaction of sulfenyl chlorides with metal trithiocarbonates, and the heptathio analog 21a was prepared similarly.Lenthionine 19 is the main product when diiodomethane is treated with sodium tetrathiopercarbonate.A rearrangement of bis(alkyltrithio)dichloromethanes 24 has been observed.Additions of sulfenyl chlorides and of thiosulfenyl chlorides to the thiocarbonyl compounds 5 and 21a were achieved in acetonitrile.The structures of the first crystalline pentathiodipercarbonate 5a and α,α,α-tris(disulfide) 29a, and of the first reported α,α,α-tris(trisulfide) 31a have been determined by X-ray crystallography.

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