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54888-34-5

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54888-34-5 Usage

Description

[(Phenylsulfinyl)methylsulfinyl]benzene, also known as dibenzylsulfoxide, is a chemical compound with the formula C14H14OS2. It is a type of sulfoxide, which contains a sulfinyl functional group. [(Phenylsulfinyl)methylsulfinyl]benzene is a colorless to pale yellow liquid with a slight sulfurous odor and is typically handled and stored under inert gas conditions to prevent oxidation. It is known for its unique steric and electronic properties, which make it a valuable reagent in organic chemistry reactions.

Uses

Used in Organic Chemistry:
[(Phenylsulfinyl)methylsulfinyl]benzene is used as a chiral auxiliary in organic chemistry for its ability to influence the stereochemistry of reactions. Its unique steric and electronic properties contribute to its effectiveness in this application.
Used in Pharmaceutical Research:
[(Phenylsulfinyl)methylsulfinyl]benzene is studied for its potential biological activities and pharmacological properties, making it a candidate for further research and development in the pharmaceutical industry.
Used in Chemical Synthesis:
As a reagent, [(Phenylsulfinyl)methylsulfinyl]benzene is utilized in the synthesis of various compounds, taking advantage of its sulfinyl functional group and its ability to act as a chiral auxiliary.
Used in Material Science:
[(Phenylsulfinyl)methylsulfinyl]benzene's unique properties may also find applications in material science, where it could be used to develop new materials with specific characteristics or to improve existing ones.

Check Digit Verification of cas no

The CAS Registry Mumber 54888-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,8 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54888-34:
(7*5)+(6*4)+(5*8)+(4*8)+(3*8)+(2*3)+(1*4)=165
165 % 10 = 5
So 54888-34-5 is a valid CAS Registry Number.

54888-34-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzenesulfinylmethylsulfinylbenzene

1.2 Other means of identification

Product number -
Other names PhSOCH2SOPh

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:54888-34-5 SDS

54888-34-5Relevant articles and documents

Meso-bis(phenylsulfinyl)methane

Kannan,Usman, Anwar,Fun, Hoong-Kun

, p. o268-o270 (2003)

The title compound, meso-C13H12O2S2, is in an anti conformation, with R and S configurations around the S atoms. The two O atoms are trans to each other, and the same applies for the two benzene rings. The pheny

Nitric acid in the presence of supported P2O5 on silica gel: An efficient and novel reagent for oxidation of sulfides to the corresponding sulfoxides

Hajipour, Abdol R.,Kooshki, Behzad,Ruoho, Arnold E.

, p. 5503 - 5506 (2007/10/03)

This paper describes an efficient and easy method for oxidation of sulfides 1 to their corresponding sulfoxides 2 with nitric acid in the presence of supported P2O5 on silica gel under solvent-free conditions in high yields.

Selective synthesis of sulfoxides and sulfones by methyltrioxorhenium-catalyzed oxidation of sulfides with hydrogen peroxide

Yamazaki, Shigekazu

, p. 2955 - 2959 (2007/10/03)

Methyltrioxorhenium-catalyzed oxidation of sulfides with hydrogen peroxide in ethanol has been found to be an efficient catalytic system for the selective formation of sulfoxides and sulfones. The oxidation using an equimolar amount of hydrogen peroxide afforded sulfoxides in excellent yield, and the use of two molar amounts of hydrogen peroxide gave sulfones quantitatively. Strongly deactivated sulfide, bis(4-nitrophenyl) sulfide, was converted smoothly to the corresponding sulfoxide and sulfone in excellent yields. The functional group in the side chain of sulfide such as a carbon-carbon double bond was not affected under the reaction conditions, and the sulfur atom was selectively oxidized.

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