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1-(3,4-dimethoxyphenyl)penta-3,4-dien-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156381-89-4

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156381-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156381-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,3,8 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156381-89:
(8*1)+(7*5)+(6*6)+(5*3)+(4*8)+(3*1)+(2*8)+(1*9)=154
154 % 10 = 4
So 156381-89-4 is a valid CAS Registry Number.

156381-89-4Relevant academic research and scientific papers

Sustainable and selective synthesis of 3,4-dihydroquinolizin-2-one and quinolizin-2-one derivatives via the reactions of penta-3,4-dien-2-ones

Fan, Xuesen,He, Yan,Zhang, Xinying,Wang, Jianji

supporting information, p. 1393 - 1398 (2014/03/21)

In this paper, a novel and green methodology for the synthesis of 3,4-dihydroquinolizin-2-one derivatives via the tandem reactions of penta-3,4-dien-2-ones with pyridine, quinoline, or isoquinoline at rt in aqueous ethanol was developed. Notably, the reac

One-pot cascade reactions of 1-arylpenta-3,4-dien-2-ones leading to 2-arylphenols and dibenzopyroanones

He, Yan,Zhang, Xinying,Fan, Xuesen

supporting information, p. 14968 - 14970 (2014/12/11)

A one-pot cascade reaction of 1-arylpenta-3,4-dien-2-ones with activated ketones allowed for an efficient and sustainable synthesis of 2-arylphenols. Moreover, this reaction was also found to be compatible and combinable with Pd-catalyzed C-H activation a

New Six- to Eight-Membered-Ring Formation Based on the Intramolecular Endo- Mode Ring Closure of Allenyl (Substituted Phenyl)alkyl Ketones

Nagao, Yoshimitsu,Lee, Woo Song,Komaki, Yoichi,Sano, Shigeki,Shiro, Motoo

, p. 597 - 600 (2007/10/02)

Several allenyl ketones possessing an aryl group were submitted to a new intramolecular endo-mode cyclization with BF3*OEt2 or TiCl4 in CH2Cl2 to afford the corresponding 6-, 7-, and 8-membered carbocyclic products.

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