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

1233720-59-6

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1233720-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1233720-59-6 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 1233720-59:
(9*1)+(8*2)+(7*3)+(6*3)+(5*7)+(4*2)+(3*0)+(2*5)+(1*9)=126
126 % 10 = 6
So 1233720-59-6 is a valid CAS Registry Number.

1233720-59-6Relevant academic research and scientific papers

Neuroprotective and Antineuroinflammatory Effects of Hydroxyl-Functionalized Stilbenes and 2-Arylbenzo[b]furans

Chen, Pei-Chun,Tsai, Wei-Jern,Ueng, Yune-Fang,Tzeng, Tsai-Teng,Chen, Hsiang-Ling,Zhu, Pei-Ru,Huang, Chia-Hsiang,Shiao, Young-Ji,Li, Wen-Tai

, p. 4062 - 4073 (2017)

The drugs currently used to treat Alzheimer’s disease (AD) are limited in the benefits they confer, and no medication has been clearly proven to cure or delay the progression of AD. Most candidate AD drugs are meant to reduce the production, aggregation,

Antioxidant activity and inhibition of α-glucosidase by hydroxyl-functionalized 2-arylbenzo[b]furans

Hsieh, Jung-Feng,Lin, Wei-Jen,Huang, Kai-Fa,Liao, Jiahn-Haur,Don, Ming-Jaw,Shen, Chien-Chang,Shiao, Young-Ji,Li, Wen-Tai

, p. 443 - 451 (2015/03/04)

This study synthesized a series of hydroxyl-functionalized 2-arylbenzo[b]furans based on the structure of tournefolic acid A and evaluated them for antioxidant and a-glucosidase inhibitory activities. Compounds 5a, 5e, and 5n showed remarkable inhibition

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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