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1726-03-0

Diphenylmethyl sulfide, also known as benzhydryl sulfide or diphenylmethyl sulfide, is an organic compound with the chemical formula C13H12S. It is a colorless to pale yellow crystalline solid that is insoluble in water but soluble in organic solvents. diphenylmethyl sulfide is formed by the linkage of two phenyl rings with a methyl group and a sulfur atom. Diphenylmethyl sulfide is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and reactivity. It can be synthesized through various methods, including the reaction of benzhydryl chloride with sodium sulfide or the condensation of thiols with benzhydryl halides. The compound is also known for its applications in the preparation of sulfoxides and sulfones, which are valuable in the field of organic chemistry.

1726-03-0

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1726-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1726-03-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1726-03:
(6*1)+(5*7)+(4*2)+(3*6)+(2*0)+(1*3)=70
70 % 10 = 0
So 1726-03-0 is a valid CAS Registry Number.

1726-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenylmethyl sulfide

1.2 Other means of identification

Product number -
Other names Dibenzhydryl-sulfid

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:1726-03-0 SDS

1726-03-0Relevant articles and documents

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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