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(E)-1-ethoxy-3-phenylthio-1-propene is an organic compound characterized by a unique structure that features a propene backbone with a phenylthio group attached to the 3-position and an ethoxy group at the 1-position. This molecule is a conjugated diene, which means it has two carbon-carbon double bonds separated by a single carbon-carbon single bond. The presence of the phenylthio group introduces a sulfur atom into the molecule, which can significantly alter its chemical reactivity and physical properties compared to its oxygen analogs. The ethoxy group provides an ether linkage, which can influence the molecule's solubility and reactivity. (E)-1-ethoxy-3-phenylthio-1-propene is of interest in organic chemistry due to its potential applications in the synthesis of various pharmaceuticals and other organic compounds, as well as its unique electronic properties that arise from the conjugation and the presence of heteroatoms.

53963-20-5

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53963-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53963-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,6 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53963-20:
(7*5)+(6*3)+(5*9)+(4*6)+(3*3)+(2*2)+(1*0)=135
135 % 10 = 5
So 53963-20-5 is a valid CAS Registry Number.

53963-20-5Downstream Products

53963-20-5Relevant academic research and scientific papers

THIOSTANNANE-MEDIATED PREPARATION OF γ-ALKOXYALLYL SULFIDES; EFFICIENT β-ALKYLATION OF α,β-UNSATURATED ALDEHYDES

Sato, Tsuneo,Okazaki, Hiroshi,Otera, Junzo,Nozaki, Hitosi

, p. 2979 - 2982 (2007/10/02)

The title β-alkylation is achieved through a sequence of sulfenylation of α-enal acetals, t-BuLi-promoted alkylation, and oxidative hydrolysis.

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