10409-07-1 Usage
Description
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.
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
10409-07-1Relevant articles and documents
Corson,Pews
, p. 1654,1655,1656,1658,1659 (1971)
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.
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Kunieda,N.,Oae,S.
, p. 233 - 234 (1968)
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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.
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
