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(Z)-2-phenylmethylene-5-methyl-7-nitro-3(2H)-benzofuranone is a complex organic compound characterized by a benzofuranone core structure. It features a phenyl group attached to the double bond (Z-configuration), a methyl group at the 5-position, and a nitro group at the 7-position. (Z)-2-phenylmethylene-5-methyl-7-nitro-3(2H)-benzofuranone is known for its potential applications in the synthesis of pharmaceuticals and other chemical products due to its unique structure and reactivity. The presence of the nitro group suggests that it may have properties related to nitroaromatic compounds, which are often used in the production of explosives, dyes, and pesticides. The specific arrangement of functional groups in this molecule can influence its chemical behavior and potential uses in various industrial and scientific applications.

84859-44-9

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84859-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84859-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,5 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84859-44:
(7*8)+(6*4)+(5*8)+(4*5)+(3*9)+(2*4)+(1*4)=179
179 % 10 = 9
So 84859-44-9 is a valid CAS Registry Number.

84859-44-9Downstream Products

84859-44-9Relevant academic research and scientific papers

Oxidative Cyclisation of Chalcones with Thallium(III)-Nitrate: Synthesis of (Z)-2-Phenylmethylene-7-nitro-3(2H)-benzofuranones

Varma, Rajender S.,Varma, Manju

, p. 1469 - 1474 (1982)

Oxidation of 2'-hydroxy-3'-nitrochalcones with thallium(III) nitrate gives (Z)-2-phenylmethylene-7-nitrobenzofuran-3(2H)-one derivatives, rather than the more usual 1,2-diaryl-3,3-dimethoxypropan-1-ones or the corresponding isoflavones. - Keywords: Oxidat

THE EFFECT OF NITRO GROUPS ON OXIDATIVE CYCLISATION OF CHALCONES BY THALLIUM(III) NITRATE(TTN)

Varma, Rajender S.,Varma, Manju

, p. 3007 - 3008 (2007/10/02)

2'-Hydroxy-3'-nitrochalcons on oxidation with thallium(III)nitrate do not give rearranged intermediates that can give isoflavons, instead cyclisation gives benzylidenebenzofuran-3(2H)-one derivates.

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