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(E)-3,4-dimethoxy-5-oxo-2-(2-oxo-4-phenylbut-3-en-1-yl)-2,5-dihydrofuran-2-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1283099-19-3

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1283099-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1283099-19-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,3,0,9 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1283099-19:
(9*1)+(8*2)+(7*8)+(6*3)+(5*0)+(4*9)+(3*9)+(2*1)+(1*9)=173
173 % 10 = 3
So 1283099-19-3 is a valid CAS Registry Number.

1283099-19-3Relevant academic research and scientific papers

Natural product-based pesticide discovery: Design, synthesis and bioactivity studies of N-amino-maleimide derivatives

Song, Xiangmin,Liu, Chunjuan,Chen, Peiqi,Zhang, Hao,Sun, Ranfeng

, (2018)

Natural products are an important source of pesticide discovery. A series of N-amino-maleimide derivatives containing hydrazone group were designed and synthesized based on the structure of linderone and methyllinderone which were isolated from Lindera erythrocarpa Makino. According to the bioassay results, compounds 2 and 3 showed 60% inhibition against mosquito (Culex pipiens pallens) at 0.25 μg·mL?1. Furthermore, the results of antifungal tests indicated that most compounds exhibited much better antifungal activities against fourteen phytopathogenic fungi than linderone and methyllinderone and some compounds exhibited better antifungal activities than commercial fungicides (carbendazim and chlorothalonil) at 50 μg·mL?1. In particular, compound 12 exhibited broad-spectrum fungicidal activity (>50% inhibitory activities against 11 phytopathogenic fungi) and compounds 12 and 14 displayed 60.6% and 47.9% inhibitory activity against Rhizoctonia cerealis at 12.5 μg·mL?1 respectively. Furthermore, compound 17 was synthesized, which lacks N-substituent at maleimide and its poor antifungal activity against Sclerotinia sclerotiorum and Rhizoctonia cerealis at 50 μg·mL?1 showed that the backbone structure of N-amino-maleimide derivatives containing hydrazone group was important to the antifungal activity.

Biomimetic total syntheses of linderaspirone A and bi-linderone and revisions of their biosynthetic pathways

Tan, Haibo,Zheng, Chao,Liu, Zheng,Wang, David Zhigang

, p. 2192 - 2195 (2011/06/25)

Chemical equations presented. Simple exposure to sunlight is sufficient for triggering photochemical [2 + 2] cycloaddition-Cope or radical rearrangement cascades in the naturally occurring methyl linderone, leading to efficient biomimetic total syntheses of linderaspirone A and bi-linderone, two recently discovered bioactive spirocyclopentenedione natural products.

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