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(E)-1-phenyl-2-((E)-styryl)diazene is an organic compound characterized by a diazenyl group (-N=N-) attached to a phenyl ring and a styryl group (a vinylbenzene moiety). This molecule exhibits a trans (E) configuration, indicating that the phenyl and styryl groups are arranged on opposite sides of the diazenyl double bond. It is a conjugated system with potential applications in the synthesis of dyes, pigments, and other organic compounds due to its extended π-electron system. The compound's chemical structure and electronic properties make it a subject of interest in the field of organic chemistry, particularly in the study of azo compounds and their derivatives.

69200-92-6

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69200-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69200-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,0 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69200-92:
(7*6)+(6*9)+(5*2)+(4*0)+(3*0)+(2*9)+(1*2)=126
126 % 10 = 6
So 69200-92-6 is a valid CAS Registry Number.

69200-92-6Downstream Products

69200-92-6Relevant academic research and scientific papers

Cobalt-catalyzed regioselective hydrohydrazination of epoxides

Liu, Xiangyu,Song, Heng,Tung, Chen-Ho,Wang, Wenguang,Zhai, Xiaofang

supporting information, p. 1572 - 1576 (2020/03/05)

Using an air-stable cobalt catalyst [Cp?Co(1,2-Ph2PC6H4S)(NCMe)]BF4 (1, Cp? = Me5C5-), we have achieved catalytic regioselective hydrohydrazination of epoxides to 1,1-hydrazinoalcohols in an atom-economical manner. The catalysis involves a cobalt-hydrazine intermediate, in which the NH2 group of the hydrazine binds to the metal center, inhibiting its nucleophilic reactivity and allowing the NH group to participate in the regioselective hydrohydrazination.

1-PHENYLAZO-1-ALKENES

Schantl, Joachim G.,Hebeisen, Paul

, p. 395 - 406 (2007/10/02)

Aliphatic aldehyde phenylhydrazones 1 were converted into 1-phenylazo-1-alkenes 3 either by the reaction with I2 and pyridine followed by base induced 1,4-elimination of pyridine.HI (Method A), or via N-(4-methylbenzenesulfonyl)-N-phenylhydrazones 7 which undergo 1,4-elimination of p-toluenesulfinic acid upon treatment with KOt-Bu (Method B).Both procedures yield mixtures of configurational isomers of the phenylazo-alkenes EE- and EZ- 3b-3e; Method B is giving rise to the kinetically controlled isomer mixture (EZ-3 predominant), which equilibrates to the thremodynamicratio (EE-3 predominant) as afforded by Method A.

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