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Bis(4-bromophenyl) sulfoxide is an organic compound with the chemical formula C12H8Br2OS. It is a derivative of bisphenol A, featuring two bromine atoms attached to the para positions of the phenyl rings. Bis(4-bromophenyl) sulfoxide is characterized by its sulfoxide functional group, which consists of a sulfur atom bonded to an oxygen atom and a phenyl group. Bis(4-bromophenyl) sulfoxide is a colorless to pale yellow solid and is soluble in organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and the presence of bromine atoms, it can be further functionalized or used in cross-coupling reactions to form a wide range of compounds with diverse applications.

1774-37-4

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1774-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1774-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1774-37:
(6*1)+(5*7)+(4*7)+(3*4)+(2*3)+(1*7)=94
94 % 10 = 4
So 1774-37-4 is a valid CAS Registry Number.

1774-37-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-(4-bromophenyl)sulfinylbenzene

1.2 Other means of identification

Product number -
Other names 4,4'-dibromodiphenyl sulphoxide

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:1774-37-4 SDS

1774-37-4Relevant academic research and scientific papers

Non-conjugated water/alcohol soluble polymers with different oxidation states of sulfide as cathode interlayers for high-performance polymer solar cells

Liu, Xi,Xu, Rongguo,Duan, Chunhui,Huang, Fei,Cao, Yong

, p. 4288 - 4295 (2016)

A series of non-conjugated water/alcohol soluble copolymers containing diphenyl sulfide, diphenyl sulfoxide or diphenyl sulfone in the main chain were synthesized. The surfactant-like functionalities in side chains endow the polymers with outstanding solubility in highly polar solvents and excellent electron extraction abilities, while the limited conjugation length of main chains renders the polymers weak optical absorption. These unique characteristics make the polymers excellent cathode interfacial layers, which contribute to highly efficient polymer solar cells (PSCs) with power conversion efficiencies of 8-9%. More importantly, some of them can yield highly efficient PSCs in a relative large interlayer thickness range of 2-20 nm. The results suggest that these polymers are promising candidates for use as cathode interfacial layers in single-junction PSCs and as recombination layers in multi-junction PSCs.

Synthesis method of sulfoxide compound

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Paragraph 0031-0033; 0047-0049, (2021/04/07)

The invention discloses a method for preparing sulfoxide derivatives with industrial application value through substituted diaryl (heterocyclic aryl) and aryl (heterocyclic aryl) alkyl sulfide compounds. Under electrochemical reaction conditions, diaryl (heterocyclic aryl) and aryl (heterocyclic aryl) alkyl sulfide compounds which are wide in source and easy to prepare and have structural diversity are used as raw materials, lithium perchlorate (LiClO4) is used as an electrolyte, acetonitrile (CH3CN) is used as a solvent, and oxygen is used as an oxidizing agent to prepare the diaryl (heterocyclic aryl) and aryl (heterocyclic aryl) alkyl sulfoxide derivatives. Compared with reported preparation methods of sulfoxide derivatives, the preparation method disclosed by the invention is green, environment-friendly, safe, energy-saving, wide in substrate application range, good in compatibility of product functional groups, easy in obtaining of raw materials and simple and convenient to operate.

Electrochemical Scalable Sulfoxidation of Sulfides with Molecular Oxygen and Water

Cheng, Zhen,Gao, Xinglian,Yao, Lingling,Wei, Zhaoxin,Qin, Guohui,Zhang, Yonghong,Wang, Bin,Xia, Yu,Abdukader, Ablimit,Xue, Fei,Jin, Weiwei,Liu, Chenjiang

, p. 3743 - 3747 (2021/07/26)

An efficient and chemoselective synthesis of sulfoxides through the electrooxidation of sulfides has been well developed. This protocol takes advantage of electricity as the terminal oxidant and of molecular oxygen and water as the oxygen atom sources. A variety of structurally diverse sulfoxide compounds are assembled in moderate to excellent yields. The scaled-up reactions at 6–20 mmol show the good practicability and application potential of this methodology. A possible free radical mechanism has been proposed to rationalize the reaction procedure.

Electrochemical oxygenation of sulfides with molecular oxygen or water: Switchable preparation of sulfoxides and sulfones

Li, Jin-Heng,Li, Yang,Sun, Qing,Xue, Qi,Zhang, Ting-Ting

supporting information, p. 10314 - 10318 (2021/12/17)

A practical and eco-friendly method for the controllable aerobic oxygenation of sulfides by electrochemical catalysis was developed. The switchable preparation of sulfoxides and sulfones was effectively controlled by reaction time, in which both molecular oxygen and water can be used as the oxygen source under catalyst and external oxidant-free conditions. The electrochemical protocol features a broad substrate scope and excellent site selectivity and is successfully applied to the modification of some sulfide-containing pharmaceuticals and their derivatives. This journal is

Emodinas a novel organic photocatalyst for selective oxidation of sulfides under mild conditions

Li, Min,Lou, Jiangli,Rao, Yijian,Yuan, Zhenbo,Zhang, Yan

, p. 19747 - 19750 (2020/06/04)

Herein, we have developed naturally-occurringEmodin, which is commercially available at low-cost, as a novel organic photocatalyst for the first time.Emodinwas successfully employed in the selective oxidation of sulfides promoted by visible-light, deliver

Switchable Synthesis of Aryl Sulfones and Sulfoxides through Solvent-Promoted Oxidation of Sulfides with O2/Air

Cheng, Zhen,Sun, Pengchao,Tang, Ailing,Jin, Weiwei,Liu, Chenjiang

, p. 8925 - 8929 (2019/11/14)

A practical and switchable method for the synthesis of aryl sulfones and sulfoxides via sulfide oxidation was developed. The chemoselectivities of products were simply controlled by reaction temperature using O2/air as the terminal oxidant and oxygen source. The broad substrate scope, easy realization of gram-scale production, and the simplification of a sulfide oxidation system render the strategy attractive and valuable.

Synthesis and nano-Pd catalyzed chemoselective oxidation of symmetrical and unsymmetrical sulfides

Li, Xing,Du, Jia,Zhang, Yongli,Chang, Honghong,Gao, Wenchao,Wei, Wenlong

, p. 3048 - 3055 (2019/03/21)

A highly chemoselective, efficient and nano-Pd catalyzed protocol for the rapid construction of sulfoxides and sulfones via the oxidation of symmetrical and unsymmetrical sulfides using H2O2 as an oxidant has been developed, respectively. The ready availability of starting materials, easy recovery and reutilization of the catalyst, wide substrate scope, and high yields make this protocol an attractive alternative. The process also involves the metal-free and microwave-promoted synthesis of symmetrical diarylsulfides, and FeCl3-mediated preparation of symmetrical diaryldisulfides through the reaction of arenediazonium tetrafluoroborates with Na2S·9H2O as a sulfur source. In addition, unsymmetrical sulfides were generated via the K2CO3-mediated reaction of arenediazonium tetrafluoroborates with symmetrical disulfides.

Method for synthesizing sulfoxide compound

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Paragraph 0076-0078, (2019/10/04)

The invention discloses a method for synthesizing a sulfoxide compound and belongs to the technical field of synthesis of organic compounds. The method disclosed by the invention comprises the step of catalyzing a reaction between a thioether compound and an oxygen gas agent under the condition of illumination by taking perylene bisimide as a catalyst, thereby obtaining the sulfoxide compound. According to the method, selective oxidation of thioether catalyzed by perylene bisimide under visible light is achieved for the first time, and sulfoxide derivatives are successfully constructed in high yield; and according to the method, the reaction conditions are mild, the reaction efficiency is high, the substrate applicable range is wide, the atom utilization ratio is high, the regioselectivity and chemical selectivity of reaction are high, and thus, the method has a potential application value.

Cercosporin-bioinspired selective photooxidation reactions under mild conditions

Li, Jia,Bao, Wenhao,Tang, Zhaocheng,Guo, Baodang,Zhang, Shiwei,Liu, Haili,Huang, Shuping,Zhang, Yan,Rao, Yijian

supporting information, p. 6073 - 6081 (2019/11/20)

The development of an efficient system for selective oxidation of organic compounds to generate more valuable compounds with molecular oxygen is a significant challenge in industrial chemistry. Bioinspired by the ability of naturally occurring perylenequinonoid pigments (PQPs) to generate reactive oxygen species (ROS) upon photoirradiation, here we report that cercosporin, one of the perylenequinonoid pigments, can function as a cost-effective and environmentally friendly photocatalyst for a wide range of selective oxidations, including benzylic C-H bonds to carbonyls, amines to aldehydes, and sulfides to sulfoxides. All of the representative reactions proceeded smoothly with high efficiency under mild conditions. Owing to the use of inexpensive metal-free visible light-driven photocatalyst produced from microbial fermentation with cheap glucose as the starting material and the ease of handling, we expect that this developed method will be particularly attractive for many more applications in synthetic transformation.

Visible-light photocatalytic aerobic oxidation of sulfides to sulfoxides with a perylene diimide photocatalyst

Gao, Yueying,Xu, Huan,Zhang, Shiwei,Zhang, Yan,Tang, Chunlei,Fan, Weizheng

supporting information, p. 7144 - 7149 (2019/08/07)

Photosensitized oxygenation has been recognised as a modern method of incorporating oxygen into a substrate, as it offers environmentally benign alternatives to several conventional synthetic procedures. A metal-free aerobic selective sulfoxidation photos

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