82136-15-0 Usage
Uses
Used in Pharmaceutical Industry:
(S)-(+)-2-(p-Toluenesulfinyl)-2-cyclopentenoneethyleneketal is used as a chiral building block for the synthesis of various biologically active molecules. Its application is crucial in the development of new drugs, as it can be incorporated into the molecular structures to impart desired properties, such as enhanced efficacy or selectivity towards specific targets.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-(+)-2-(p-Toluenesulfinyl)-2-cyclopentenoneethyleneketal is utilized as a reagent in asymmetric synthesis. This allows for the creation of enantiomerically pure compounds, which can be essential for the development of effective and environmentally friendly agrochemicals with minimal off-target effects.
Used in Organic Synthesis:
(S)-(+)-2-(p-Toluenesulfinyl)-2-cyclopentenoneethyleneketal is employed as a versatile intermediate in organic synthesis, where its unique reactivity and selectivity are harnessed to facilitate the preparation of complex organic molecules. This makes it a valuable tool for chemists working on the design and synthesis of novel compounds with potential applications in various fields, including materials science, pharmaceuticals, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 82136-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,3 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82136-15:
(7*8)+(6*2)+(5*1)+(4*3)+(3*6)+(2*1)+(1*5)=110
110 % 10 = 0
So 82136-15-0 is a valid CAS Registry Number.
82136-15-0Relevant articles and documents
Asymmetric Induction during Organometallic Conjugate Addition to Enantiomerically Pure 2-(Arylsulfinyl)-2-cyclopentenones
Posner, Gary H.,Mallamo, John P.,Hulce, Martin,Frye, Leah L.
, p. 4180 - 4185 (2007/10/02)
Virtually complete asymmetric induction is achieved during methyl-, vinyl- and naphthylmetallic conjugate addition to enantiomerically pure (S)-(+)-2-(p-tolylsulfinyl)-2-cyclopentenone ((S)-(+)-1). (R)-3-Methylcyclopentanone is obtained when the enone sul
