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Bis(2,4-dichlorobenzyl) sulfide, also known as 2,4-dichlorobenzyl disulfide, is an organic compound with the chemical formula C14H12Cl4S2. It is a colorless to pale yellow crystalline solid that is insoluble in water but soluble in organic solvents. bis(2,4-dichlorobenzyl) sulfide is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential use as a pesticide and has been studied for its insecticidal properties. Due to its chemical structure, bis(2,4-dichlorobenzyl) sulfide exhibits a high degree of reactivity and can undergo various chemical transformations, making it a versatile building block in organic synthesis.

6295-41-6

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6295-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6295-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6295-41:
(6*6)+(5*2)+(4*9)+(3*5)+(2*4)+(1*1)=106
106 % 10 = 6
So 6295-41-6 is a valid CAS Registry Number.

6295-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dichloro-1-[(2,4-dichlorophenyl)methylsulfanylmethyl]benzene

1.2 Other means of identification

Product number -
Other names 2.4.2'.4'-Tetrachlor-dibenzylsulfid

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:6295-41-6 SDS

6295-41-6Relevant academic research and scientific papers

Araliphatic sulfonium and their use

-

, (2008/06/13)

Sulfonium salts of the formulae I to IV STR1 in which A is C1 -C12 alkyl, C3 -C8 cycloalkyl, C4 -C10 cycloalkylalkyl, phenyl which is unsubstituted or mono- or polysubstituted by C1 -C8 alkyl, C1 -C4 alkoxy, halogen, nitro, phenyl, phenoxy, alkoxycarbonyl having 1-4 C atoms in the alkoxy radical or acyl having 1-12 C atoms, Ar, Ar1 and Ar2, independently of one another, are each unsubstituted or mono- or polysubstituted phenyl, or naphthyl which is unsubstituted or mono- or polysubstituted each arylene is an unsubstituted or mono- or polysubstituted phenylene or unsubstituted or mono- or polysubstituted naphthylene and Q? is SbF6-, AsF6- or SbF5 OH- are valuable curing agents and curing accelerators in the heat-curing of cationically polymerizable compounds, preferably epoxy resins.

Desulfurization of benzylic mercaptans by triiron dodecacarbonyl under acidic and biphasic conditions

Alper, Howard,Sibtain, Fazle

, p. 225 - 229 (2007/10/02)

The biphasic reaction of benzylic mercaptans with triiron dodecacarbonyl, 48-50% tetrafluoroboric acid, and benzene affords desulfurized products in good to excellent yields. This reaction is superior to that effected in the presence of sodium dodecylbenzenesulfonate, a phase transfer agent for acidic processes.

PHASE TRANSFER CATALYZED DESULFURIZATION REACTIONS

Alper, Howard,Sibtain, Fazle,Heveling, Josef

, p. 5329 - 5332 (2007/10/02)

Mercaptans react with triiron dodecarbonyl or dicobalt octacarbonyl, under phase transfer catalysis conditions, to give hydrocarbons in good yields.

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