84428-15-9 Usage
Description
Ethyl 3-(3-Hydroxy-4-Methoxyphenyl)-2-propenoate, with the CAS number 84428-15-9, is an off-white solid compound that is useful in organic synthesis. It is characterized by its unique chemical structure, which includes a hydroxy and methoxy substituent on a phenyl ring, and an ester functional group.
Uses
Used in Organic Synthesis:
Ethyl 3-(3-Hydroxy-4-Methoxyphenyl)-2-propenoate is used as a synthetic intermediate for the production of various organic compounds. Its unique chemical structure allows it to be a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
Ethyl 3-(3-Hydroxy-4-Methoxyphenyl)-2-propenoate is used as a key intermediate in the synthesis of pharmaceutical compounds. Its presence in the molecule can impart specific biological activities, making it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
Ethyl 3-(3-Hydroxy-4-Methoxyphenyl)-2-propenoate is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique structure can contribute to the effectiveness of these products in controlling pests and weeds.
Used in Specialty Chemicals:
Ethyl 3-(3-Hydroxy-4-Methoxyphenyl)-2-propenoate is used as a raw material in the production of specialty chemicals, such as dyes, fragrances, and flavorings. Its chemical properties can be utilized to create unique and desirable characteristics in these products.
Check Digit Verification of cas no
The CAS Registry Mumber 84428-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,2 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84428-15:
(7*8)+(6*4)+(5*4)+(4*2)+(3*8)+(2*1)+(1*5)=139
139 % 10 = 9
So 84428-15-9 is a valid CAS Registry Number.
84428-15-9Relevant articles and documents
Hypervalent-Iodine(III)-Mediated Tandem Oxidative Dearomatization/Aziridination of Phenolic Amines: Synthesis of Functionalized Unactivated Aziridines
Cao, Ye-Xing,Silalai, Patamawadee,Liu, Chun-Fang,Yu, Ke-Yin,Bao, Xu,Zhao, Xian-He,Saeeng, Rungnapha,Fan, Chun-An
supporting information, p. 8473 - 8478 (2021/05/17)
A new hypervalent-iodine(III)-mediated tandem reaction involving oxidative dearomatization and in situ aziridination of phenolic amines is described, providing a mild and effective method for the assembly of structurally interesting and synthetically usef
Synthesis and anticancer activities of glycyrrhetinic acid derivatives
Li, Yang,Feng, Ling,Song, Zhi-Fang,Li, Hai-Bei,Huai, Qi-Yong
, (2016/05/09)
A total of forty novel glycyrrhetinic acid (GA) derivatives were designed and synthesized. The cytotoxic activity of the novel compounds was tested against two human breast cancer cell lines (MCF-7, MDA-MB-231) in vitro by the MTT method. The evaluation results revealed that, in comparison with GA, compound 42 shows the most promising anticancer activity (IC50 1.88 ± 0.20 and 1.37 ± 0.18 μM for MCF-7 and MDA-MB-231, respectively) and merits further exploration as a new anticancer agent.
Synthesis of some phenylpropanoid glycosides (PPGs) and their acetylcholinesterase/xanthine oxidase inhibitory activities
Li, Xiao-Dong,Kang, Shuai-Tao,Li, Guo-Yu,Li, Xian,Wang, Jin-Hui
experimental part, p. 3580 - 3596 (2011/07/07)
In this research, three categories of phenylpropanoid glycosides (PPGs) were designed and synthesized with PPGs isolated from Rhodiola rosea L. as lead compounds. Their inhibitory abilities toward acetylcholinesterase (AChE) and xanthine oxidase (XOD) were also tested. Some of the synthetic PPGs exhibited excellent enzyme inhibitory abilities.
