105378-41-4 Usage
Uses
As the specific properties and uses of 2,4,6-Octatrienoic acid, 4-(phenylseleno)-, ethyl ester are not widely documented, it is difficult to provide a comprehensive list of its applications. However, based on the information provided, we can infer the following potential uses:
Used in Organic Synthesis:
2,4,6-Octatrienoic acid, 4-(phenylseleno)-, ethyl ester is used as a reagent for [application reason] in organic synthesis due to its unique structure and the presence of the phenylseleno group.
Used in Chemical Reactions:
2,4,6-Octatrienoic acid, 4-(phenylseleno)-, ethyl ester is used as a reagent for [application reason] in various chemical reactions, potentially due to its ability to participate in reactions involving the phenylseleno group.
Check Digit Verification of cas no
The CAS Registry Mumber 105378-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,7 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105378-41:
(8*1)+(7*0)+(6*5)+(5*3)+(4*7)+(3*8)+(2*4)+(1*1)=114
114 % 10 = 4
So 105378-41-4 is a valid CAS Registry Number.
105378-41-4Relevant academic research and scientific papers
Syntheses d'alcools allyliques et alleniques fonctionnels a partir de composes carbonyles α-phenylselenies
Lerouge, Patrice,Paulmier, Claude
, p. 1225 - 1229 (2007/10/02)
The functionalized allylic selenides 6, 7, 8, 10 and 11 were prepared from phenylselenoaldehydes and ketones 1, and phenylselenopyruvates 2 using the Wittig or the Horner reaction. 2,3-Sigmatropic rearrangement of the corresponding selenoxides leads to the functional allylic alcohols 15, 16 and 17 and to the conjugated enals 18, 19 and 20.A method for the conversion of an aldehyde into the enal with an additional carbon is described.The functional 3-phenylselenobutadienes 23, 24 and 25 were also obtained from α-phenylselenoenals 21 in the same manner.An oxidation-rearrangement reaction appears to be a convenient way to prepare the functional or substitued allenic alcohols 26 and 28.The ethyl 2-hydroxy pent-3,4-dienoate 26c has been cyclized by benzeneselenenyl bromide into the ethyl 2,5-dihydrofurancarboxylate 29.
