40918-88-5 Usage
Uses
Used in Pharmaceutical Industry:
(2E)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2E)-3-(3,4-dimethoxyphenyl)prop-2-enoate is used as a potential pharmaceutical compound for [application reason]. Its unique molecular structure may offer specific benefits in drug development, such as enhancing the efficacy of certain medications or improving their delivery to target sites within the body.
Used in Industrial Applications:
In the industrial sector, (2E)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2E)-3-(3,4-dimethoxyphenyl)prop-2-enoate is used as a component in [application type] for [application reason]. Its properties may contribute to the development of new materials or processes that improve upon existing technologies or create novel applications.
Check Digit Verification of cas no
The CAS Registry Mumber 40918-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,1 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40918-88:
(7*4)+(6*0)+(5*9)+(4*1)+(3*8)+(2*8)+(1*8)=125
125 % 10 = 5
So 40918-88-5 is a valid CAS Registry Number.
40918-88-5Relevant academic research and scientific papers
Synthesis and biological evaluation of a natural ester sintenin and its synthetic analogues
Hu, Li Hong,Zou, Hong Bin,Gong, Jing Xu,Li, Hai Bo,Yang, Lei Xiang,Cheng, Wei,Zhou, Chang Xin,Bai, Hua,Gueritte, Francoise,Zhao, Yu
, p. 342 - 348 (2007/10/03)
Synthesis of 3-(3,4-dimethoxyphenyl)propyl-3-(3,4-dimethoxyphenyl) propanoate (18), a cytotoxic natural ester, was carried out by a convenient synthetic path with a total yield of 49%. Sixteen of its analogues (19-34) were also prepared. Seventeen unsaturated derivatives of 18, compounds 1-17, were also synthesized to examine the structure-activity relationship of this type of ester. All of the synthetic compounds were passed through the cytotoxicity screenings on human tumor cell lines, such as PC-3, Hela, A549, BEL7404, CNE, and KB. Some of the esters exhibited moderate inhibitory effects on these tumor cell lines. The phenolic derivatives exhibited the highest cytotoxicity among these derivatives, while the unsaturated esters were more cytotoxic than the saturated analogues. Some of the compounds also exhibited inhibition on α-glucosidase.
