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Top quality factory supply 10409-07-1 Bis-(p-tolyl)-disulfone at low price
- Molecular Formula: C14H14 O4 S2
- Molecular Weight: 310.395
- Vapor Pressure: 7.07E-09mmHg at 25°C
- Melting Point: 212 °C
- Boiling Point: 479.1°C at 760 mmHg
- Flash Point: 300.5°C
- PSA: 85.04000
- Density: 1.329g/cm3
- LogP: 4.62760
Bis-(p-tolyl)-disulfone(Cas 10409-07-1) Usage
|
General Description |
Bis-(p-tolyl)-disulfone is a chemical compound with the molecular formula C14H12O2S2. It is a white to light yellow powder that is insoluble in water but soluble in organic solvents. Bis-(p-tolyl)-disulfone is commonly used as an intermediate in the production of dyes, polymers, and pharmaceuticals. It is also used as a cross-linking agent in the manufacturing of rubber and plastics. Bis-(p-tolyl)-disulfone is known for its ability to enhance the heat resistance and stability of various materials, making it a valuable additive in the production of heat-resistant polymers and coatings. However, it is important to handle this compound with care, as it may cause irritation to the skin, eyes, and respiratory system upon exposure. |
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
10409-07-1 Relevant articles
Direct conversion of sulfinic acid to sulfonic acid derivatives
Furukawa,Nishikawa,Inaba,et al.
, p. 623 - 628 (1981)
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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 bas...
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/...
-
Kunieda,N.,Oae,S.
, p. 233 - 234 (1968)
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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 ...
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 prov...
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 di...
10409-07-1 Process route
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19481-79-9
2-iodo-2-methylpropanenitrile
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1950-78-3
p-toluenesulfonyl iodide
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10409-07-1
bis(4-methylphenyl)disulfone
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2943-42-2
di(4-methyl)phenylthiosulfonate
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4124-41-8
p-toluenesulfonylanhydride
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98039-88-4
1-cyano-1-methylethyl p-tolyl sulphone
| Conditions | Yield |
|---|---|
|
With
copper;
In
tetrachloromethane;
for 6h;
Heating;
|
7.1%
|
-
-
1950-78-3
p-toluenesulfonyl iodide
-
-
103-19-5
di(p-tolyl) disulfide
-
-
10409-07-1
bis(4-methylphenyl)disulfone
-
-
2943-42-2
di(4-methyl)phenylthiosulfonate
-
-
4124-41-8
p-toluenesulfonylanhydride
| Conditions | Yield |
|---|---|
|
With
2,2'-azobis(isobutyronitrile);
In
tetrachloromethane;
for 9h;
Further byproducts given;
Heating;
|
1.52 g
1.21 g 2.03 g 1.81 g |
10409-07-1 Upstream products
-
10439-23-3
4-methylbenzenesulfinyl chloride
-
67-66-3
chloroform
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536-57-2
p-toluene sulfinic acid
-
60-29-7
diethyl ether
10409-07-1 Downstream products
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103-19-5
di(p-tolyl) disulfide
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2943-42-2
di(4-methyl)phenylthiosulfonate
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536-57-2
p-toluene sulfinic acid
-
104-15-4
toluene-4-sulfonic acid
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