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2-Propenal, 3-[3,4-bis(acetyloxy)phenyl]-, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

402761-80-2

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402761-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 402761-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,7,6 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 402761-80:
(8*4)+(7*0)+(6*2)+(5*7)+(4*6)+(3*1)+(2*8)+(1*0)=122
122 % 10 = 2
So 402761-80-2 is a valid CAS Registry Number.

402761-80-2Relevant academic research and scientific papers

DDQ-mediated oxidation of allylarenes: Expedient access to cinnamaldehyde-containing phenylpropanoids

Jiang, Tao-Shan,Zhang, Qingqing,Li, Guohui,Cheng, Xi,Cai, Yongping

, p. 4611 - 4616 (2018)

Phenylpropanoid natural products containing a cinnamaldehyde motif were easily synthesized from allylarenes mediated by 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) oxidation. Representative examples described herein are five types of 4-hydroxycinnamaldehyde derivatives from monolignols biosynthesis, Boropinal C, and 7-methoxywutaifuranal from plant extracts. Especially, simple synthesis of 7-methoxywutaifuranal was exploited through selective mono-oxidation and subsequent isomerization-ring-closing-metathesis strategy.

One step of palladium catalyzed benzodioxane ring C-O bond formation, synthesis of isoamericanol A and isoamericanin A

Jing, Xiaobi,Shi, Yaocheng,Liu, Yonghong,Han, Ying,Yan, Chaoguo,Wang, Li

, p. 1723 - 1727 (2007/10/03)

A number of benzodioxane compounds were synthesized using the palladium-catalyzed etherification of aryl halides by employing triphenylphosphane ligands. This method was used as key step in the synthesis of two natural products isoamericanol A and isoamericanin A.

Chemical syntheses of caffeoyl and 5-OH coniferyl aldehydes and alcohols and determination of lignin o-methyltransferase activities in dicot and monocot species

Chen, Fang,Kota, Parvathi,Blount, Jack W.,Dixon, Richard A.

, p. 1035 - 1042 (2007/10/03)

To investigate the substrate preferences of O-methyltransferases in the monolignol biosynthetic pathways, caffeoyl and 5-hydroxy coniferyl aldehydes were synthesized by a new procedure involving a Wittig reaction with the corresponding hydroxybenzaldehydes. The same procedure can also be used to synthesize caffeoyl and 5-hydroxyconiferyl alcohols. Relative O-methyltransferase activities against these substrates were determined using crude extracts and recombinant caffeic acid O-methyltransferase from alfalfa (Medicago sativa), and crude extracts from the model legume. Medicago truncatula, tobacco, wheat and tall fescue. Extracts from all these species catalyzed methylation of the various monolignol aldehydes and alcohols more effectively than the corresponding hydroxycinnamic acids.

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