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The chemical compound "Benzopyrano(5,4,3-cde)(1)benzopyrano(5,4,3-cde)(1)benzopyran-5,10-dione, 2,3,7,8-tetrakis(acetyloxy)-" is a complex organic molecule characterized by its unique structure. It features a benzopyrano-fused benzopyrano-benzopyran core, which is a type of polycyclic aromatic compound. The compound is further defined by the presence of four acetyloxy groups attached at the 2, 3, 7, and 8 positions, which contribute to its reactivity and potential applications. This specific arrangement of functional groups and the polycyclic structure endow the molecule with distinct chemical properties, making it a subject of interest in organic chemistry and potentially in various industrial applications, such as in the synthesis of pharmaceuticals or other specialty chemicals.

4274-26-4

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4274-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4274-26-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4274-26:
(6*4)+(5*2)+(4*7)+(3*4)+(2*2)+(1*6)=84
84 % 10 = 4
So 4274-26-4 is a valid CAS Registry Number.

4274-26-4Downstream Products

4274-26-4Relevant academic research and scientific papers

Anti-babesial and anti-plasmodial compounds from Phyllanthus niruri

Subeki,Matsuura, Hideyuki,Takahashi, Kosaku,Yamasaki, Masahiro,Yamato, Osamu,Maede, Yoshimitsu,Katakura, Ken,Kobayashi, Sumiko,Trimurningsih,Chairul,Yoshihara, Teruhiko

, p. 537 - 539 (2005)

Bioassay-guided fractionation of boiled aqueous extracts from the whole plant of Phyllanthus niruri led to the isolation of 1-O-galloyl-6-O-luteoyl- α-D-glucose (1), with IC50 values of 4.7 μg/mL against Babesia gibsoni and 1.4 μg/mL against Plasmodium falciparum in vitro. The known compounds β-glucogallin (2), quercetin 3-O-β-D-glucopyranosyl- (2→1)-O-β-D-xylopyranoside (3), β-sitosterol, and gallic acid were also isolated. Structures of these compounds were elucidated on the basis of their chemical and spectroscopic data.

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