40807-05-4 Usage
Description
(E)-2-(3-nitrophenyl)ethenyl phenyl sulfone, with the molecular formula C14H9NO4S, is a yellow crystalline chemical compound that boasts a molecular weight of 287.29 g/mol. This versatile compound is characterized by its unique structure and properties, which make it a valuable asset in the realm of organic chemistry. Its ability to participate in a range of chemical reactions, including nucleophilic addition, oxidation, and reduction, underscores its potential for diverse applications.
Uses
Used in Organic Synthesis:
(E)-2-(3-nitrophenyl)ethenyl phenyl sulfone is utilized as a reagent in organic synthesis, where its capacity to engage in various chemical reactions is highly beneficial. Its versatility in this context allows for the creation of a wide array of products, contributing to the compound's significance in the field.
Used in Pharmaceutical Development:
The unique structure and properties of (E)-2-(3-nitrophenyl)ethenyl phenyl sulfone render it a promising candidate for the development of pharmaceuticals. Its ability to undergo multiple chemical reactions enables the synthesis of a variety of compounds with potential therapeutic applications.
Used in Agrochemical Production:
In addition to its pharmaceutical applications, (E)-2-(3-nitrophenyl)ethenyl phenyl sulfone is also employed in the production of agrochemicals. Its chemical reactivity and structural uniqueness make it a valuable component in the development of new and improved products for the agricultural industry.
Used in the Construction of Functional Materials:
(E)-2-(3-nitrophenyl)ethenyl phenyl sulfone serves as a building block for the construction of various functional materials. Its chemical properties and reactivity contribute to the creation of materials with specific characteristics, making it a valuable resource in material science and engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 40807-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,0 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40807-05:
(7*4)+(6*0)+(5*8)+(4*0)+(3*7)+(2*0)+(1*5)=94
94 % 10 = 4
So 40807-05-4 is a valid CAS Registry Number.
40807-05-4Relevant articles and documents
Method for synthesizing (E)-(2-(phenylsulfonyl)vinyl)benzene and derivative thereof
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Paragraph 0049-0050, (2018/07/30)
The invention provides a method for synthesizing (E)-(2-(phenylsulfonyl)vinyl)benzene and a derivative thereof. The method adopts styrene or a derivative of styrene as a reactant A and sodium benzenesulfinate or a derivative of sodium benzenesulfinate as
Visible-Light-Enabled Decarboxylative Sulfonylation of Cinnamic Acids with Sulfonylhydrazides under Transition-Metal-Free Conditions
Cai, Shunyou,Xu, Yaohui,Chen, Danling,Li, Lihuang,Chen, Qifa,Huang, Mingqiang,Weng, Wen
supporting information, p. 2990 - 2993 (2016/07/06)
Decarboxylative cross-coupling reactions of cinnamic acids with sulfonylhydrazides were explored using oxygen as the sole terminal oxidant, realizing a conceptually novel technology for vinyl sulfone synthesis under the synergistic interactions of visible light irradiation, organic dye-type photocatalyst eosin Y, KI, and Cs2CO3 at room temperature.
Convenient synthesis of α,β-unsaturated sulfones via a Mizoroki-Heck reaction of arylboronic acids with phenyl vinyl sulfones
Kabalka, George W.,Guchhait, Sankar K.
, p. 4021 - 4022 (2007/10/03)
Palladium acetate catalyzed Mizoroki-Heck reaction of arylboronic acids with phenyl vinyl sulfones afford α,β-unsaturated sulfones in good yields.
