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Bis-(p-tolyl)-disulfone, with the molecular formula C14H12O2S2, is a white to light yellow powder that is insoluble in water but soluble in organic solvents. It is a versatile chemical compound used as an intermediate in the production of various materials due to its ability to enhance heat resistance and stability.

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  • 10409-07-1 Structure
  • Basic information

    1. Product Name: Bis-(p-tolyl)-disulfone
    2. Synonyms: Bis-(p-tolyl)-disulfone
    3. CAS NO:10409-07-1
    4. Molecular Formula: C14H14O4S2
    5. Molecular Weight: 310.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10409-07-1.mol
  • Chemical Properties

    1. Melting Point: 212 °C
    2. Boiling Point: 479.1°C at 760 mmHg
    3. Flash Point: 300.5°C
    4. Appearance: /
    5. Density: 1.329g/cm3
    6. Vapor Pressure: 7.07E-09mmHg at 25°C
    7. Refractive Index: 1.586
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Bis-(p-tolyl)-disulfone(CAS DataBase Reference)
    11. NIST Chemistry Reference: Bis-(p-tolyl)-disulfone(10409-07-1)
    12. EPA Substance Registry System: Bis-(p-tolyl)-disulfone(10409-07-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10409-07-1(Hazardous Substances Data)

10409-07-1 Usage

Uses

Used in Chemical Production:
Bis-(p-tolyl)-disulfone is used as an intermediate in the production of dyes, polymers, and pharmaceuticals, contributing to the development of a wide range of products across different industries.
Used in Rubber and Plastics Industry:
Bis-(p-tolyl)-disulfone is used as a cross-linking agent in the manufacturing of rubber and plastics, improving the mechanical properties and durability of these materials.
Used in Heat-Resistant Polymers and Coatings:
Bis-(p-tolyl)-disulfone is used as an additive in the production of heat-resistant polymers and coatings, enhancing their thermal stability and resistance to high temperatures, making them suitable for various applications where high heat is involved.
It is important to handle Bis-(p-tolyl)-disulfone with care, as it may cause irritation to the skin, eyes, and respiratory system upon exposure. Proper safety measures should be taken during its use to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 10409-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,0 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10409-07:
(7*1)+(6*0)+(5*4)+(4*0)+(3*9)+(2*0)+(1*7)=61
61 % 10 = 1
So 10409-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O4S2/c1-11-3-7-13(8-4-11)19(15,16)20(17,18)14-9-5-12(2)6-10-14/h3-10H,1-2H3

10409-07-1SDS

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 4,4'-Dimethyldiphenyldisulfone

1.2 Other means of identification

Product number -
Other names di-p-tolyl disulphone

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:10409-07-1 SDS

10409-07-1Relevant articles and documents

Bromonitromethane, a Versatile Electrophile: Reactions with Feebly Basic Nucleophiles

Fishwick, Brian R.,Rowles, David K.,Stirling, Charles J. M.

, p. 835 - 836 (1983)

Bromonitromethane reacts with feebly basic sulphur, phosphorus, and halogen nucleophiles at bromine or at carbon; the anion of bromonitromethane reacts with tributylboron to give 1-nitropentane.

Electrochemical Sulfonylation/Heteroarylation of Alkenes via Distal Heteroaryl ipso-Migration

Zheng, Ming-Wei,Yuan, Xin,Cui, Yu-Sheng,Qiu, Jiang-Kai,Li, Guigen,Guo, Kai

, p. 7784 - 7789 (2018)

A direct electrooxidative sulfonylation/heteroarylation reaction of alkenes with sulfinic acids, which proceeds through distal heteroaryl ipso-migration and C-S and C-C bond formations, is reported. This electro-synthetic method offers an efficient and en

Synthesis of Symmetrical Thiosulfonates via Cu(OTf)2-Catalyzed Reductive Homocoupling of Arenesulfonyl Chlorides

Liu, Lixia,Luo, Bo,Wang, Chengming

supporting information, p. 5880 - 5883 (2021/11/27)

A variety of symmetrical thiosulfonates are synthesized via Cu-catalyzed reductive homocoupling of aryl sulfonyl chlorides. This protocol uses organic amine acting as a mild reductant and low-cost copper as an effective catalyst. Such a reductive coupling process features a broad substrate scope and good functional group tolerance. Related thiosulfonate products can also be converted into diverse functional molecules.

Phenylboronic acid-catalyzed tandem construction of S-S and C-S bonds: a new method for the synthesis of benzyl disulfanylsulfone derivatives fromS-benzyl thiosulfonates

Jannapu Reddy, Raju,Rama Krishna, Gamidi,Waheed, Md.

, p. 3243 - 3248 (2020/05/14)

A unique phenylboronic acid-catalyzed dimerization-sulfonylation ofS-benzyl thiosulfonates has been disclosed. A metal-free tandem construction of S-S and C-S bonds is an operationally simple method to access a wide range of benzyl disulfanylsulfone derivatives in high to excellent yields. Moreover, the robustness of this tandem transformation has been demonstrated by gram-scale reactions, and a plausible mechanism is also proposed.

N,N′-Disulfonylhydrazines: New sulfonylating reagents for highly efficient synthesis of (E)-vinyl sulfones at room temperature

Hu, Yuefei,Luo, Dongping,Min, Lin,Shan, Lidong,Wang, Xinyan,Zheng, Weiping

, (2020/02/18)

N,N′-Disulfonylhydrazines have been proven to be the most reactive precursors of sulfonyl radicals in all types of sulfonyl substituted hydrazines as early as a half century ago. But such function has not been applied in organic synthesis except the formation of disulfones by self-dimerization of sulfonyl radicals. In this article, they were introduced as new sulfonylating reagents and their combinations with NIS and Et3N were established as excellent iodosulfonylating reagents for alkenes. Finally, a highly efficient method for the synthesis of (E)-vinyl sulfones was developed by mixing an alkene, a N,N′-disulfonylhydrazine, NIS and Et3N in THF at room temperature for 5 min.

Electrochemical oxidation of sulfinic acids: Efficient oxidative synthesis of diaryl disulfones

Nematollahi, Davood,Joudaki, Mahsa,Khazalpour, Sadegh,Pouladi, Firozeh

, p. G65 - G70 (2017/08/26)

Electrochemical oxidation of sulfinic acids has been studied in aqueous solutions using cyclic voltammetry, controlled-potential coulometry, chronoamperometry and chronocoulometry methods. The results indicate that the oxidation of sulfinic acids is an ir

A paradigm shift in rate determining step from single electron transfer between phenylsulfinylacetic acids and iron(III) polypyridyl complexes to nucleophilic attack of water to the produced sulfoxide radical cation: a non-linear Hammett

Subramaniam, Perumal,Janet Sylvia Jaba Rose, Jebamoney,Jeevi Esther Rathinakumari, Rajasingh

, p. 496 - 504 (2016/09/21)

Mechanism of oxidative decarboxylation of phenylsulfinylacetic acids (PSAAs) by iron(III) polypyridyl complexes in aqueous acetonitrile medium has been investigated spectrophotometrically. An initial intermediate formation between PSAA and [Fe(NN)3]3+ is confirmed from the observed Michaelis–Menten kinetics and fractional order dependence on PSAA. Significant rate retardation with concentration of [Fe(NN)3]3+ is rationalized on the basis of coordination of a water molecule at the carbon atom adjacent to the ring nitrogen of the metal polypyridyl complexes by nucleophilic attack at higher concentrations. Electron-withdrawing and electron-releasing substituents in PSAA facilitate the reaction and Hammett correlation gives an upward ‘V’ shaped curve. The apparent upward curvature is rationalized based on the change in the rate determining step from electron transfer to nucleophilic attack, by changing the substituents from electron-releasing to electron-withdrawing groups. Electron-releasing substituents in PSAA accelerate the electron transfer from PSAA to the complex and also stabilize the intermediate through resonance interaction leading to negative reaction constants (ρ). Conversely, electron-withdrawing groups, while retarding the electron transfer exert an accelerating effect on the nucleophilic attack of H2O which leading to low magnitude of ρ+ compared to high ρ? values of electron-releasing groups. Marcus theory is applied, and a fair agreement is seen with the experimental values. Copyright

Facile preparation of bis(thiocarbonyl)disulfides via elimination

Weber, Wolfgang G.,McLeary, James B.,Sanderson, Ron D.

, p. 4771 - 4774 (2007/10/03)

A robust facile synthetic preparation of bis(thiocarbonyl)disulfides is presented. The route follows an elimination mechanism rather than the more common oxidation. Addition of p-tosyl chloride to a thiocarbonyl thiolate results in the elimination of the chloride by the trithiocarbonate anion and subsequent elimination of the tosyl leaving group (by a second thiocarbonyl thiolate). The side products of the reaction are bis(4-methylphenyl)disulfone and tosylate salts/acids.

Temperature-controlled selective reduction of arenesulfonyl chlorides promoted by samarium metal in DMF

Liu, Yongjun,Zhang, Yongmin

, p. 4291 - 4294 (2007/10/03)

Promoted by samarium in DMF, arenesulfonyl chlorides can be selectively reduced to diaryldisulfones, diarylthiosulfonates and diaryldisulfides in good to excellent yields by reaction temperature control without the need to pretreat or activate the metallic samarium.

Sonochemical Preparation of Aromatic α-Disulfones

Prokes, Ivan,Toma, Stefan,Luche, Jean-Louis

, p. 3849 - 3850 (2007/10/02)

Reasonable yields (60-70percent) of aromatic α-disulfones can be obtained in short reaction times from a sonicated mixture of an arenesulfonyl chloride and lithium in THF. - Key Words: Alpha-disulfones, sonication, Wurtz-type coupling

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