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6-methoxy-6-phenyl-6H-chromeno[3,4-b]quinoxaline is a complex organic compound characterized by a unique molecular structure. It belongs to the class of quinoxaline derivatives, which are known for their diverse applications in pharmaceuticals, agrochemicals, and materials science. This particular compound features a quinoxaline core, which is fused with a chromene ring, and is further adorned with a methoxy group at the 6-position and a phenyl group at the 6-position as well. The presence of these functional groups endows the molecule with specific chemical properties and potential reactivity. The compound's structure and properties make it a subject of interest for researchers exploring new synthetic pathways and potential applications in various fields.

1808-06-6

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1808-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1808-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,0 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1808-06:
(6*1)+(5*8)+(4*0)+(3*8)+(2*0)+(1*6)=76
76 % 10 = 6
So 1808-06-6 is a valid CAS Registry Number.

1808-06-6Downstream Products

1808-06-6Relevant academic research and scientific papers

Reactions of Flav-2-enes and Flav-2-en-4-ones (Flavones)

Bird, T. Geoffrey C.,Brown, Ben R.,Stuart, Ian A.,Tyrrell, William R.

, p. 1831 - 1846 (2007/10/02)

Flav-2-enes, flavones, and 3-alkyl ethers of flavonols add alcohols and carboxylic acids in the presence of N-bromosuccinimide to give 2-alkoxy- and 2-acyloxy-3-bromoflavans which provide routes to cis-3-bromoflavans by reduction and to 3,4-diols by elimination and reaction with osmium tetraoxide.The 2-acyloxyflavans react with alcohols yielding 2-alkoxyflavans.Flavonols react with N-bromosuccinimide and alcohols to give bromine-free hemiacetals, the known 2,3-dialkoxy-3-hydroxyflavanones.

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