226089-80-1 Usage
Description
2-(1,3-Dioxolan-2-yl)benzyl phenyl sulfone is a chemical compound with the molecular formula C15H14O3S. It is a white to off-white crystalline powder that is insoluble in water but soluble in organic solvents. The presence of a dioxolane ring in its structure makes it a versatile intermediate in organic synthesis, and it has been used in the production of a wide range of other chemical compounds.
Uses
Used in Pharmaceutical Industry:
2-(1,3-Dioxolan-2-yl)benzyl phenyl sulfone is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
2-(1,3-Dioxolan-2-yl)benzyl phenyl sulfone is also used as a building block for the synthesis of agrochemicals. Its versatility in organic synthesis enables the creation of new compounds with potential applications in agriculture.
Used as a Corrosion Inhibitor:
2-(1,3-Dioxolan-2-yl)benzyl phenyl sulfone has been studied for its potential application as a corrosion inhibitor. Its properties may offer protection against corrosion in various industrial applications.
Used in Organic Synthesis:
The presence of a dioxolane ring in the structure of 2-(1,3-Dioxolan-2-yl)benzyl phenyl sulfone makes it a versatile intermediate in organic synthesis. It has been used in the production of a wide range of other chemical compounds, contributing to the development of new materials and products.
Check Digit Verification of cas no
The CAS Registry Mumber 226089-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,0,8 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 226089-80:
(8*2)+(7*2)+(6*6)+(5*0)+(4*8)+(3*9)+(2*8)+(1*0)=141
141 % 10 = 1
So 226089-80-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O4S/c17-21(18,14-7-2-1-3-8-14)12-13-6-4-5-9-15(13)16-19-10-11-20-16/h1-9,16H,10-12H2
226089-80-1Relevant articles and documents
Integrated Chemical Process: One-Pot Double Elimination Method for Acetylenes
Orita, Akihiro,Yoshioka, Naonori,Struwe, Petra,Braier, Arnold,Beckmann, Anke,Otera, Junzo
, p. 1355 - 1363 (2007/10/03)
A novel one-pot process for synthesis of acetylenes has been achieved in which the following series of steps are integrated: addition of an α-anion of sulfone to aldehyde; trapping of the resulting adduct to incorporate a leaving group, and double elimination of this intermediate. Consolidation of Peterson elimination renders the process much simpler. This method provides a convenient and high-yielding access to a variety of enynes and polyynes as well as to functionally substituted aryl acetylenes containing halogen(s) or acetal groups, which are useful building blocks for aryl acetylene scaffolds. Iteration of the one-pot generation of acetylenic bonds provides a new metodology for the buildup of aryl acetylene skeletons.
