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1H-Naphth[2,3-g]indole-6,11-dione, 3-benzoyl-5-hydroxy-2-phenyl- is a complex organic compound with the molecular formula C24H15NO4. It is characterized by a naphthindole core, which is a fused ring system consisting of a naphthalene and an indole. The compound features a 3-benzoyl group, which is a benzoyl moiety attached to the third carbon of the naphthindole, and a 5-hydroxy group, indicating the presence of a hydroxyl group at the fifth position. Additionally, it has a 2-phenyl substituent, meaning a phenyl group is attached to the second carbon of the naphthindole. 1H-Naphth[2,3-g]indole-6,11-dione, 3-benzoyl-5-hydroxy-2-phenyl- is known for its potential applications in the field of pharmaceuticals and materials science, particularly in the development of novel therapeutic agents and advanced materials.

90656-07-8

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90656-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90656-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,5 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90656-07:
(7*9)+(6*0)+(5*6)+(4*5)+(3*6)+(2*0)+(1*7)=138
138 % 10 = 8
So 90656-07-8 is a valid CAS Registry Number.

90656-07-8Downstream Products

90656-07-8Relevant academic research and scientific papers

REACTION OF BORATE COMPLEXES OF 1,4-DIAMINO- AND 1-AMINO-4-HYDROXYANTHRAQUINONES WITH THE ANIONS OF CH ACIDS

Gorelik, M. V.,Mishina, E. V.

, p. 1892 - 1899 (2007/10/02)

The reaction of the diboroacetates of 1,4-diamino- and 1-amino-4-hydroxyanthraquinones with CH acids in an aprotic polar solvent in the presence of a base leads to the angular 5-amino- and 5-hydroxynaphtoindole-6,11-diones respectively.In the reaction of the diboroacetate of 2,3-dichloro-1,4-diaminoanthraquinone with dibenzoylmethane the main reaction product is the linear 4,11-diaminoanthrafuran-5,10-dione.

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