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1,2-bis(4-chlorophenyl)disulfane 1,2-dioxide, also known as 4,4'-dichlorodiphenylsulfone, is an organic compound with the chemical formula C12H8Cl2O2S2. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. 1,2-bis(4-chlorophenyl)disulfane 1,2-dioxide is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a building block for the production of polymers and resins. Due to its chemical structure, it exhibits thermal stability and resistance to hydrolysis, making it a valuable component in the development of high-performance materials.

6275-39-4

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6275-39-4 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This classifies the compound as a disulfane dioxide, which is a type of sulfur-containing compound.

Explanation

The presence of these groups contributes to the compound's chemical properties and reactivity.

Explanation

The compound serves as a starting material or a building block for synthesizing other organic compounds.

Explanation

The compound is utilized in the production of various chemicals, including those used in agriculture and medicine.

Explanation

The compound's appearance and solid state at room temperature.

Explanation

The temperature range at which the compound transitions from a solid to a liquid state.

Explanation

The compound's chemical properties make it valuable in various industries and for scientific research.

Disulfane dioxide derivative

Contains two sulfur atoms bonded to each other and two oxygen atoms.

Contains two 4-chlorophenyl groups

Each phenyl group has four chlorine atoms.

Used in organic synthesis

Key intermediate in the production of certain organic compounds.

Applications in manufacturing

Pesticides and pharmaceuticals.

Physical state

White crystalline solid.

Melting point

183-185°C.

Chemical properties

Important for industrial applications and research purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 6275-39-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6275-39:
(6*6)+(5*2)+(4*7)+(3*5)+(2*3)+(1*9)=104
104 % 10 = 4
So 6275-39-4 is a valid CAS Registry Number.

6275-39-4SDS

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 1-chloro-4-(4-chlorophenyl)sulfinylsulfinylbenzene

1.2 Other means of identification

Product number -
Other names 4,4'-Dichlor-diphenyldisulfoxid

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:6275-39-4 SDS

6275-39-4Downstream Products

6275-39-4Relevant academic research and scientific papers

Silver nitrate catalyzed oxidation of sulfides

Das, Rima,Chakraborty, Debashis

experimental part, p. 277 - 280 (2011/03/18)

A variety of sulfides were converted into the corresponding sulfoxide derivatives with 70% tert-butyl hydroperoxide in water as the oxidant in the presence of catalytic quantity of silver nitrate. The method described has a wide range of application, does not involve cumbersome workup, exhibits chemoselectivity, and proceeds under mild reaction conditions, and the resulting products are obtained in good yields within a reasonable time. Georg Thieme Verlag Stuttgart New York.

Cu(II)-catalyzed oxidation of sulfides

Das, Rima,Chakraborty, Debashis

scheme or table, p. 6255 - 6258 (2011/01/04)

A variety of sulfides and disulfides were converted into the corresponding sulfoxide derivatives with 70% t-BuOOH (water) as the oxidant in the presence of catalytic quantity of CuBr2. The method described does not involve cumbersome work-up, has wide range of applicabilities, exhibits chemoselectivity, and proceeds under mild reaction conditions, and the resulting products are obtained in good yields within reasonable time.

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