96649-50-2 Usage
Description
4-[2-(2,6-Dimethoxy-phenoxy)-ethyl]-piperazin-1-yl-furan-2-yl-methanone is a complex organic compound featuring a piperazine ring and a furan ring connected to a methanone group. The molecule also includes a phenoxyethyl group substituted with two methoxy groups. This unique structure hints at possible pharmacological applications, as similar compounds are often utilized in the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
4-[2-(2,6-Dimethoxy-phenoxy)-ethyl]-piperazin-1-yl-furan-2-yl-methanone is used as a potential pharmaceutical compound for its unique chemical structure. The presence of a piperazine ring and a furan ring, along with the methanone group and the phenoxyethyl group with methoxy substituents, suggests that this compound may have valuable biological properties. Further research and testing are required to determine its specific applications and effectiveness in the pharmaceutical field.
Used in Chemical Research:
In the field of chemical research, 4-[2-(2,6-Dimethoxy-phenoxy)-ethyl]-piperazin-1-yl-furan-2-yl-methanone can be used as a starting material or a model compound for studying the properties and reactivity of similar structures. This can contribute to the development of new synthetic methods, understanding of reaction mechanisms, and the discovery of novel compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 96649-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,6,4 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96649-50:
(7*9)+(6*6)+(5*6)+(4*4)+(3*9)+(2*5)+(1*0)=182
182 % 10 = 2
So 96649-50-2 is a valid CAS Registry Number.
96649-50-2Relevant articles and documents
Structure-Activity Relationships for Prazosin and WB 4101 Analogues as α1-Adrenoreceptor Antagonists
Giardina, Dario,Bertini, Rosaria,Brancia, Egle,Brasili, Livio,Melchiorre, Carlo
, p. 1354 - 1357 (1985)
Several α-adrenoreceptor antagonists were prepared by coupling one of the two moieties of WB 4101 (1) with one of the two moieties of prazosin (2).Their blocking activity and relative selectivity on α1- and α2-adrenoreceptors were evaluated in the isolated rat vas deferens.Although retaining a significant selectivity toward α1-adrenoreceptors, all the drugs were weaker antagonists than the parent compounds 1 and 2.Opening the piperazine ring of 2 gave 3, which displayed a very high activity and selectivity toward α1-adrenoreceptors (α1/α2 = 3890).This may have relevance in understanding the mode of action of prazosin.In addition, 3 may represent a valuable tool in the characterization of α-adrenoreceptor subtypes.
