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Ethanone, 1-(3-bromo-2,4,6-trimethoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29784-38-1

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29784-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29784-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,8 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29784-38:
(7*2)+(6*9)+(5*7)+(4*8)+(3*4)+(2*3)+(1*8)=161
161 % 10 = 1
So 29784-38-1 is a valid CAS Registry Number.

29784-38-1Downstream Products

29784-38-1Relevant academic research and scientific papers

Synthesis of novel organohalogen chalcone derivatives and screening of their molecular docking study and some enzymes inhibition effects

Burmaoglu, Serdar,Kazancioglu, Elif Akin,Kaya, Ruya,Kazancioglu, Mustafa,Karaman, Muhammet,Algul, Oztekin,Gulcin, Ilhami

, (2020)

Chalcones and their derivatives are increasing attention due to numerous biochemical and pharmacological applications. In this study, a series of novel organohalogen chalcone derivatives (5–12) were tested towards α-glycosidase (α-Gly), acetylcholinestera

Fusing privileged structures: Synthesis and characterization of new benzothiophene-chalcone hybrids

Kazancioglu, Elif Akin

, (2021/11/17)

Chalcones form the core of a variety of medicinal compounds which possess a wide variety of cytoprotective and modulatory therapeutic potential for multiple disease states. A series of benzothiophene-chalcone hybrids were designed and prepared through the

A new method for halogenation of aromatic compounds by using dimethyldioxirane and tetrabutylammonium halides

Lee, Yean-Jang,Wu, Huan-Ting,Lin, Chia-Ning

experimental part, p. 585 - 587 (2010/04/23)

In this presentation the novel regioselective halogenation of arenes or phenols with dimethyldioxirane and Bu4NX is described. The results showed that a new, versatile and mild method can be utilized for preparation of aryl halides starting with arenes or phenols. Finally, this aryl halide forming methodology is applicable to structurally more complex flavonoids.

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