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3,6-Diethenyl-9-ethyl-9H-carbazole is a chemical compound with the molecular formula C17H15N. It is a derivative of the parent compound carbazole, which is a tricyclic aromatic hydrocarbon consisting of a dibenzopyrrole structure. The presence of two vinyl groups (C2H3) at the 3 and 6 positions, along with an ethyl group (C2H5) at the 9 position, distinguishes 9H-Carbazole, 3,6-diethenyl-9-ethyl- from its parent structure. This specific arrangement of functional groups may influence its chemical properties and potential applications, such as in the synthesis of advanced materials or as intermediates in organic chemistry.

1592-64-9

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1592-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1592-64-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1592-64:
(6*1)+(5*5)+(4*9)+(3*2)+(2*6)+(1*4)=89
89 % 10 = 9
So 1592-64-9 is a valid CAS Registry Number.

1592-64-9Downstream Products

1592-64-9Relevant articles and documents

A convenient synthesis of 3,6-substituted carbazoles via nickel catalyzed cross-coupling

Park, Minnie,Buck, Jason R.,Rizzo, Carmelo J.

, p. 12707 - 12714 (2007/10/03)

Alkyl, vinyl and aryl substitiuted carbazoles at the 3- and 6-positions are prepared in high yield from the corresponding 3,6-dibromocarbazole via nickel catalyzed coupling with Grignard reagents (Corriu-Kumada coupling).

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