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(E)-1-Phenyl-4-phenylselanyl-pent-2-en-1-one is an organic compound characterized by a pent-2-en-1-one backbone, which features a carbonyl group at the 1st position and a double bond between the 2nd and 3rd carbon atoms. The molecule is further distinguished by a phenyl group attached to the 1st carbon and a phenylselanyl group (a phenyl group bonded to a selenium atom) at the 4th carbon. This arrangement gives the compound a unique structure with potential applications in various chemical and pharmaceutical contexts. The "E" configuration indicates that the phenyl and phenylselanyl groups are on opposite sides of the double bond, which is important for understanding its stereochemistry.

91925-38-1

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91925-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91925-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,2 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91925-38:
(7*9)+(6*1)+(5*9)+(4*2)+(3*5)+(2*3)+(1*8)=151
151 % 10 = 1
So 91925-38-1 is a valid CAS Registry Number.

91925-38-1Relevant academic research and scientific papers

PROPRIETES DES α-PHENYLSELENOALDEHYDES REACTIONS DE WITTIG CONDUISANT A DES α-HYDROXYESTERS ET CETONES β,γ-ETHYLENIQUES ET A DES ALDEHYDES α,β-ETHYLENIQUES

Lerouge, Patrice,Paulmier, Claude

, p. 1983 - 1986 (2007/10/02)

Wittig and Wittig-Horner reactions with α-phenylselenoaldehydes lead to allylic selenides.The corresponding selenoxides undergo 2,3-sigmatropic rearrangement providing a route to α-hydroxy β,γ-ethylenic esters and ketones in good yields.In a some way, we prepare, also enals with an additional carbon.

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