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10-[(E)-Cyclohexylimino]-4-hydroxy-1-phenylamino-10H-anthracen-9-one is a complex organic compound characterized by its anthracene-based structure. This molecule features a cyclohexylimino group at the 10th position, which is in the E configuration, indicating the geometric arrangement of the double bond. Additionally, it has a hydroxyl group at the 4th position and a phenylamino group at the 1st position, both of which contribute to its chemical reactivity and properties. The compound is part of the anthraquinone family, known for its diverse applications in various industries, including pharmaceuticals and dyes. Its specific structure endows it with unique chemical and physical characteristics, making it a subject of interest in chemical research and development.

83989-99-5

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83989-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83989-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,8 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83989-99:
(7*8)+(6*3)+(5*9)+(4*8)+(3*9)+(2*9)+(1*9)=205
205 % 10 = 5
So 83989-99-5 is a valid CAS Registry Number.

83989-99-5Downstream Products

83989-99-5Relevant academic research and scientific papers

1-HYDROXY-9,10-ANTHRAQUINONE 9-ALKYLIMINES AND THEIR CONVERSION INTO 1,3-OXAZINOANTHRONES

Popov, S.I.,Volosenko, V.P.

, p. 1708 - 1712 (2007/10/02)

A series of previously uninvestigated N-alkyl-substituted 1-hydroxyanthraquinone 9-imines were obtained.In an acidic medium they decompose to hydroxyanthraquinone, but the 4-amino derivatives are stable to acid hydrolysis.In polar solvents in the presence of bases the 1-hydroxy-9,10-anthraquinone 9-alkylimines undergo intramolecular cyclization to derivatives of anthra-1,3-oxazinoanthrones.

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