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2-((E)-1-Phenyl-oct-3-ene-4-sulfinyl)-pyridine is a complex organic chemical compound characterized by a pyridine ring, which is a six-membered aromatic ring containing two nitrogen atoms. The compound features a phenyl group (a benzene ring with a hydrogen atom replaced by a phenyl group) attached to an oct-3-ene chain, which is an eight-carbon alkene chain with a double bond between the third and fourth carbon atoms. The "E" configuration indicates that the phenyl group and the sulfinyl group are on opposite sides of the double bond. The sulfinyl group (-SO) is attached to the fourth carbon of the oct-3-ene chain, and the entire structure is connected to the pyridine ring at the 2-position. 2-((E)-1-Phenyl-oct-3-ene-4-sulfinyl)-pyridine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

77063-39-9

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77063-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77063-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,6 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77063-39:
(7*7)+(6*7)+(5*0)+(4*6)+(3*3)+(2*3)+(1*9)=139
139 % 10 = 9
So 77063-39-9 is a valid CAS Registry Number.

77063-39-9Relevant academic research and scientific papers

HIGHLY STEREOSELECTIVE SYNTHESIS OF TRISUBSTITUTED OLEFINS FROM ALKENYL ARYL SULFOXIDES

Takei, Hisashi,Sugimura, Hideyuki,Miura, Morikazu,Okamura, Hisashi

, p. 1209 - 1212 (2007/10/02)

Alkenyl aryl sulfoxides could be alkylated stereoselectively via their lithium salts to afford α-alkylated (E)-alkenyl sulfoxides.Reduction of the sulfoxides to the corresponding sulfides followed by nickel-phosphine complexes catalyzed coupling reaction

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