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1-Phenylnaphtho[2,1-b]furan-2(1H)-one is a complex organic compound characterized by a unique molecular structure. It features a naphthofuran core, which is a fusion of a naphthalene ring and a furan ring, with a phenyl group attached to the naphthalene. 1-phenylnaphtho[2,1-b]furan-2(1H)-one is known for its potential applications in various chemical and pharmaceutical industries, particularly in the synthesis of certain drugs and dyes. Its chemical formula is C17H10O2, indicating the presence of 17 carbon atoms, 10 hydrogen atoms, and 2 oxygen atoms. The compound's structure and properties make it a subject of interest for researchers exploring the synthesis and applications of complex aromatic systems.

6670-63-9

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6670-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6670-63-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,7 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6670-63:
(6*6)+(5*6)+(4*7)+(3*0)+(2*6)+(1*3)=109
109 % 10 = 9
So 6670-63-9 is a valid CAS Registry Number.

6670-63-9Downstream Products

6670-63-9Relevant academic research and scientific papers

Gold-catalyzed chemoselective formal (3+2)-Annulation reaction between β-naphthols and methyl aryldiazoacetate

Harada, Shingo,Sakai, Chigaya,Tanikawa, Koki,Nemoto, Tetsuhiro

, p. 3650 - 3656 (2019/06/05)

A chemoselective domino annulation reaction of β-naphthols with methyl aryldiazoacetate is described. The gold catalyst promoted C–H functionalization of β-naphthols, whereas a rhodium or copper complex led to O–H insertion reactions. Consecutive intramol

Generation and intramolecular cyclization of (2- ethenylphenyl)bisketenes. Synthesis of benzofuranones

Heileman, Matthew J.,Moore, Harold W.

, p. 3643 - 3646 (2007/10/03)

Several new differentially substituted cyclobutenediones 4a-e have been prepared. Their thermal rearrangement to substituted naphthofuranones 5a-d is reported. This rearrangement involves an unprecedented intramolecular cyclization of a reactive bisketene 6, and forms the naphthofuranone system in good yield.

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