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(4-Methoxy-3,5-dimethyl-phenyl)-(4-nitro-phenyl)-diazene is a complex organic compound characterized by its unique molecular structure. It features a diazenyl functional group, which is a nitrogen-nitrogen double bond, connecting two distinct phenyl rings. One phenyl ring is substituted with a 4-methoxy group and two methyl groups at the 3 and 5 positions, while the other phenyl ring bears a 4-nitro group. (4-Methoxy-3,5-dimethyl-phenyl)-(4-nitro-phenyl)-diazene is notable for its potential applications in the synthesis of various chemical products, such as dyes and pharmaceuticals, due to its reactive diazenyl group and the presence of electron-donating and electron-withdrawing substituents on the phenyl rings. The compound's properties, such as its reactivity and stability, are influenced by the electronic effects of these substituents, making it a subject of interest in organic chemistry research and development.

34267-76-0

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34267-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34267-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,6 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34267-76:
(7*3)+(6*4)+(5*2)+(4*6)+(3*7)+(2*7)+(1*6)=120
120 % 10 = 0
So 34267-76-0 is a valid CAS Registry Number.

34267-76-0Downstream Products

34267-76-0Relevant academic research and scientific papers

Evaluation of Through-Space Interaction in Metacyclophanes by Diazo Coupling Reaction

Tsuge, Akihiko,Moriguchi, Tetsuji,Mataka, Shuntaro,Tashiro, Masashi

, p. 2211 - 2216 (2007/10/02)

An azobenzene moiety was introduced into various metacyclophanes (MCPs) 1 via diazo coupling reactions.The functional groups on the inner (8,16-) or outer (13-) positions affect the reactivity of the outer (5-) position toward the diazonium salts to

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