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8H-1,3-Dioxolo[4,5-g][1]benzopyran-8-one, 6,7-dihydro-6-phenyl- is a complex organic compound with the molecular formula C14H10O4. It is a derivative of benzopyran, which is a heterocyclic compound consisting of a benzene ring fused to a pyran ring. The compound features a 1,3-dioxolo ring, which is a five-membered ring containing two oxygen atoms, and a phenyl group attached to the 6-position. This specific structure is known for its potential applications in the synthesis of various pharmaceuticals and natural products, particularly those with biological activity. The compound's unique arrangement of atoms and functional groups may contribute to its reactivity and properties, making it a subject of interest in organic chemistry and drug development.

4388-66-3

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4388-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4388-66-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4388-66:
(6*4)+(5*3)+(4*8)+(3*8)+(2*6)+(1*6)=113
113 % 10 = 3
So 4388-66-3 is a valid CAS Registry Number.

4388-66-3Downstream Products

4388-66-3Relevant academic research and scientific papers

Synthesis of Flavanones via Palladium(II)-Catalyzed One-Pot β-Arylation of Chromanones with Arylboronic Acids

Cho, Yang Yil,Jang, Hyu Jeong,Kim, Dong Hwan,Kim, Nam Yong,Kim, Nam-Jung,Kim, Young Min,Lee, Soo Jin,Lee, Yong Sup,Park, Boyoung Y.,Son, Seung Hwan,Yoo, Hyung-Seok

, p. 10012 - 10023 (2019/08/30)

A total of 47 flavanones were expediently synthesized via one-pot β-arylation of chromanones, a class of simple ketones possessing chemically unactivated β sites, with arylboronic acids via tandem palladium(II) catalysis. This reaction provides a novel route to various flavanones, including natural products such as naringenin trimethyl ether, in yields up to 92percent.

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