66826-89-9 Usage
General Description
[(2-phenylcyclopropyl)sulfonyl]benzene is a chemical compound with a molecular formula C15H14O2S. It consists of a benzene ring with a sulfonyl group attached to a phenylcyclopropyl ring. [(2-phenylcyclopropyl)sulfonyl]benzene is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential use as a precursor in the development of new organic materials and as an intermediate in the synthesis of biologically active molecules. The compound's unique structure and reactivity make it a valuable tool in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 66826-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,2 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66826-89:
(7*6)+(6*6)+(5*8)+(4*2)+(3*6)+(2*8)+(1*9)=169
169 % 10 = 9
So 66826-89-9 is a valid CAS Registry Number.
66826-89-9Relevant articles and documents
Synthesis of substituted tetrahydrofurans via intermolecular reactions of γ-chlorocarbanions of 3-substituted 3-chloro-propylphenyl sulfones with aldehydes
Brandt, Agnieszka,Wojtasiewicz, Anna,?niezek, Marcin,Makosza, Mieczys?aw
experimental part, p. 3378 - 3385 (2010/06/20)
Carbanions of 3-substituted-3-chloropropyl phenyl sulfones add to carbonyl groups of aldehydes to produce aldol type adducts that undergo 1,5-intramolecular substitution giving 2,3,5-trisubstituted tetrahydrofurans. The effect of substituents in the 3-pos
Reactivity of bifunctional olefins with hydrazine hydrate - Part II
Bhaskar Reddy,Rajagopal Sarma,Somasekhar Reddy,Subba Reddy
, p. 901 - 903 (2007/10/03)
The reaction of 1-aroyl-2-arylsulfonylethenes 1 with different ratios of hydrazine hydrate lead to hydrazones, dimerized products and 2-pyrazolines. The reactivity of pyrazolines has also been studied by dehydrogenation, pyrolysis, nitrosation and acylation.