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(4-Methoxy-phenyl)-xanthen-9-ylidene-amine is a complex organic compound with the molecular formula C20H15NO2. It is characterized by a xanthene core, which is a tricyclic aromatic system consisting of two benzene rings fused to a pyran ring. The compound features a 4-methoxy-phenyl group attached to the xanthene, which contributes to its electronic properties and potential applications. The 9-position of the xanthene is substituted with an amide group, forming a ylidene structure. This chemical is known for its potential use in the synthesis of dyes and other organic compounds, and it may also have implications in the field of materials science due to its unique structure and properties.

79751-94-3

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79751-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79751-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,5 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79751-94:
(7*7)+(6*9)+(5*7)+(4*5)+(3*1)+(2*9)+(1*4)=183
183 % 10 = 3
So 79751-94-3 is a valid CAS Registry Number.

79751-94-3Upstream product

79751-94-3Downstream Products

79751-94-3Relevant academic research and scientific papers

Iminodimagnesium Reagents. Condensation Reaction with Ketones. Direct Preparation of Anils and a Hydrazone of Xanthone

Okubo, Masao,Hayashi, Saeko,Matsunaga, Mayumi,Uematsu, Yumiko

, p. 2337 - 2340 (1981)

The condensation reaction of ketones with iminodimagnesium reagents (RN(MgBr)2) derived from various primary amines as well as 1,1-disubstituted hydrazines was investigated.A-Arylimines and 1-methyl-1-phenylhydrazones of diaryl ketones were prepared, thei

The thermal and photolytic decomposition of 9-aryl-9-xanthenyl azides to 11-aryldibenzo[b,f][1,4] oxazepines

Coombes, Philip,Goosen, Andre,Taljaard, Benjamin

, p. 559 - 563 (2007/10/02)

In contrast to the different ratios of products obtained in the thermal decomposition of some 9-aryl-9-xanthenyl azides, it was found that photolysis afforded the same product ratio. The mechanism of these reactions is discussed in terms of intermediates as well as conformational and electronic effects in the transition states.

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