Welcome to LookChem.com Sign In|Join Free

CAS

  • or

31515-43-2

Post Buying Request

31515-43-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

31515-43-2 Usage

General Description

2-Nitrophenyl phenyl sulfone is a chemical compound with the molecular formula C12H9NO3S. It is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. 2-Nitrophenyl phenyl sulfone is commonly used as a reactant in organic synthesis and as a photoinitiator in photopolymerization processes. 2-Nitrophenyl phenyl sulfone has been found to exhibit anti-inflammatory and analgesic properties, and it is also used as a starting material in the production of dyes, optical brighteners, and pharmaceuticals. Additionally, it has been studied for its potential use in materials science and as a corrosion inhibitor for metals.

Check Digit Verification of cas no

The CAS Registry Mumber 31515-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,1 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31515-43:
(7*3)+(6*1)+(5*5)+(4*1)+(3*5)+(2*4)+(1*3)=82
82 % 10 = 2
So 31515-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO4S/c14-13(15)11-8-4-5-9-12(11)18(16,17)10-6-2-1-3-7-10/h1-9H

31515-43-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (469009)  2-Nitrophenylphenylsulfone  97%

  • 31515-43-2

  • 469009-1G

  • 618.93CNY

  • Detail

31515-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Nitrophenyl phenyl sulfone

1.2 Other means of identification

Product number -
Other names 2-NITROPHENYL PHENYL SULPHONE

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:31515-43-2 SDS

31515-43-2Relevant articles and documents

Selective synthesis of sulfoxides and sulfonesviacontrollable oxidation of sulfides withN-fluorobenzenesulfonimide

Cao, Zhong-Yan,Li, Xiaolong,Lu, Hao,Wang, Panpan,Wang, Shengqiang,Xu, Xiaobo,Yan, Leyu,Yang, A-Xiu

supporting information, p. 8691 - 8695 (2021/10/22)

A practical and mild method for the switchable synthesis of sulfoxides or sulfonesviaselective oxidation of sulfides using cheapN-fluorobenzenesulfonimide (NFSI) as the oxidant has been developed. These highly chemoselective transformations were simply achieved by varying the NFSI loading with H2O as the green solvent and oxygen source without any additives. The good functional group tolerance makes the strategy valuable.

Silver-promoted decarboxylative sulfonylation of aromatic carboxylic acids with sodium sulfinates

Yu, Yongqi,Wu, Qianlong,Liu, Da,Yu, Lin,Tan, Ze,Zhu, Gangguo

, p. 11195 - 11202 (2019/09/12)

A novel and efficient synthesis of sulfones was developed via a silver-promoted decarboxylative sulfonylation reaction between aromatic carboxylic acids and sodium sulfinates for the first time. The approach features operational simplicity and good functional group compatibility and uses readily available starting materials. Furthermore, mechanistic studies reveal that the decarboxylative sulfonylation reaction is likely to proceed via a radical mechanism.

Carbon-supported metal-modified lacunary tungstosilicic polyoxometallates used as catalysts in the selective oxidation of sulfides

Frenzel, Romina,Sathicq, ángel G.,Blanco, Mirta N.,Romanelli, Gustavo P.,Pizzio, Luis R.

, p. 27 - 36 (2015/04/14)

Lacunary tungstosilicic polyoxometallates modified with transition metal ions [SiW11O39M(H2O)]6-, where M = Mn2+, Fe2+, Co2+or Cu2+, were synthesized and supported on activated carbon to obtain the SiW11MC catalysts. The samples were characterized by FT-IR, XRD, N2 adsorption-desorption measurements, and the acidic properties were determined using the isopropanol dehydration test reaction. The activity and selectivity of the catalysts were evaluated in the selective oxidation of a series of sulfides to sulfoxides or sulfone. The reaction was carried out in acetonitrile as solvent using H2O2 35% p/V as a clean oxidant. The conversion values decreased in the following order: SiW11MnC > SiW11FeC > SiW11CuC > SiW11CoC. The catalysts were reused without appreciable loss of their catalytic activity. It was found that the activity of the catalysts decreases in parallel with the increment in the reduction temperature values. The most easily reducible catalyst displayed the highest conversion values. We found a convenient and selective procedure for oxidizing sulfides to sulfoxides or sulfones using aqueous hydrogen peroxide and a catalytic amount of lacunary tungstosilicic polyoxometallates supported on carbon at low temperatures (20-50 °C) in a reasonably short reaction time

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 31515-43-2