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2-(3,4-methylenedioxystyryl)-4-bromo-6-methoxyphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1233720-58-5

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1233720-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1233720-58-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,7,2 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1233720-58:
(9*1)+(8*2)+(7*3)+(6*3)+(5*7)+(4*2)+(3*0)+(2*5)+(1*8)=125
125 % 10 = 5
So 1233720-58-5 is a valid CAS Registry Number.

1233720-58-5Relevant academic research and scientific papers

2-Phenylbenzo[b]furans: Synthesis and promoting activity on estrogen biosynthesis

Pu, Wenchen,Yuan, Yun,Lu, Danfeng,Wang, Xin,Liu, Hanwei,Wang, Chun,Wang, Fei,Zhang, Guolin

, p. 5497 - 5500 (2016)

Estrogen biosynthesis is pivotal to many physiological processes of human. Aberrant estrogen level is closely related to a variety of diseases, including breast cancer and osteoporosis. Previously we found that 2-phenylbenzo[b]furan glycosides could promote estrogen biosynthesis. To find high active 2-phenylbenzo[b]furans, fifty-four 2-phenylbenzo[b]furans were prepared via four strategies according to corresponding substrate scopes. Biological evaluation in HEK293A cells showed that some compounds exhibited promotive activity on estrogen biosynthesis. 2-(4-Chlorophenyl)-7-methoxybenzo[b]furan possessed the highest activity with EC50value of 14.68?μM. Furthermore, these compounds did not affect aromatase expression in HEK292A cells, indicating that these 2-phenylbenzo[b]furans might enhance estrogen biosynthesis via directly allosteric regulation of aromatase or indirectly via posttranslational modification.

Total synthesis of ailanthoidol, egonol, and related analogues

Duan, Xin-Fang,Shen, Gang,Zhang, Zhan-Bin

experimental part, p. 1181 - 1187 (2010/06/12)

Efficient and general synthetic protocols were developed for the total synthesis of ailanthoidol, egonol, and some related analogues. The key transformations describe here involve a two-step construction of the benzofuran and a Sonogashira coupling, and proved to be convenient and effective, starting from readily available reagents.

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