15753-89-6 Usage
Description
[(ethenylsulfonyl)methyl]benzene, also known as vinylsulphonylmethylbenzene, is a chemical compound characterized by its molecular formula C9H10OS. It presents as a colorless to pale yellow liquid and is predominantly utilized in the production of specific polymers and resins. Additionally, it serves as a starting material in the synthesis of a variety of organic compounds. Classified as a reactive chemical, it necessitates careful handling to prevent potential skin and eye irritation upon contact. Inhalation or ingestion may also pose health risks, emphasizing the importance of adhering to safety guidelines and precautions when working with this substance.
Uses
Used in Polymer and Resin Production:
[(ethenylsulfonyl)methyl]benzene is used as a key component in the production of certain polymers and resins. Its unique chemical properties contribute to the formation of these materials, enhancing their structural integrity and performance characteristics.
Used in Organic Synthesis:
This chemical compound is also employed as a starting material in the synthesis of various organic compounds. Its versatile reactivity allows for the creation of a wide range of products, making it a valuable asset in the field of organic chemistry.
Used in Chemical Research:
Due to its reactive nature and potential for use in the synthesis of multiple compounds, [(ethenylsulfonyl)methyl]benzene is also utilized in chemical research. It aids in the exploration of new chemical reactions and the development of novel substances with potential applications across various industries.
Used in Pharmaceutical Industry:
While not explicitly mentioned in the provided materials, the potential applications of [(ethenylsulfonyl)methyl]benzene in the pharmaceutical industry could include its use as an intermediate in the synthesis of pharmaceutical compounds, leveraging its reactivity to create new drugs or drug candidates.
Used in Chemical Manufacturing:
In the broader chemical manufacturing industry, [(ethenylsulfonyl)methyl]benzene may be used as an intermediate or additive in the production of various chemicals, taking advantage of its reactive properties to create a diverse array of products.
Check Digit Verification of cas no
The CAS Registry Mumber 15753-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,5 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15753-89:
(7*1)+(6*5)+(5*7)+(4*5)+(3*3)+(2*8)+(1*9)=126
126 % 10 = 6
So 15753-89-6 is a valid CAS Registry Number.
15753-89-6Relevant articles and documents
Difluoro- and trifluoro diazoalkanes-complementary approaches in batch and flow and their application in cycloaddition reactions
Hock, Katharina J.,Mertens, Lucas,Metze, Friederike K.,Schmittmann, Clemens,Koenigs, Rene M.
, p. 905 - 909 (2017/08/14)
Herein we report on applications of fluorinated diazoalkanes in cycloaddition reactions, with the emphasis on studying subtle differences between diverse fluorinated diazo compounds. These differences led to two major synthetic protocols in batch and flow that allow the safe and scalable synthesis of fluoroalkyl-, sulfone-substituted pyrazolines.
The epoxy-Ramberg-Baecklund reaction (ERBR): A sulfone-based method for the synthesis of allylic alcohols
Evans, Paul,Johnson, Paul,Taylor, Richard J. K.
, p. 1740 - 1754 (2007/10/03)
The epoxy-Ramberg-Baecklund reaction (ERBR) is outlined, in which α,β-epoxy sulfones are converted into a range of mono-, di- and tri-substituted allylic alcohols, on treatment with base. Modification of this method enabled the preparation of enantio-enriched allylic alcohols following the diastereoselective epoxidation of enantio-enriched vinyl sulfones that were accessed efficiently from the chiral pool. The scope, optimisation and limitations of the ERBR as a method for the preparation of allylic alcohols are discussed. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.
The Epoxy-Ramberg-Backlund reaction: A new route to allylic alcohols
Evans, Paul,Taylor, Richard J. K.
, p. 3055 - 3058 (2007/10/03)
A new variant of the Ramberg-Backlund reaction is described, the epoxy-Ramberg-Backlund reaction (ERBR), in which α,β-epoxysulfones, on treatment with base, are converted into a range of mono-, di- and tri-substituted allylic alcohols. The scope and limitations of the ERBR are discussed.
