1015-97-0 Usage
Physical appearance
Yellow crystalline solid The compound appears as yellow, crystalline solid structures.
Solubility
Insoluble in water, soluble in organic solvents 1H-Benz[f]indazole-4,9-dione does not dissolve in water but can dissolve in certain organic solvents.
Chemical class
Benzindazole The compound belongs to the benzindazole class of chemicals, which is a group of organic compounds with a specific chemical structure.
Applications
Organic synthesis and medicinal chemistry research 1H-Benz[f]indazole-4,9-dione is commonly used in the synthesis of organic materials and for research in medicinal chemistry.
Pharmacological properties
Anti-inflammatory and antitumor activities The compound has been studied for its potential therapeutic effects, including reducing inflammation and inhibiting tumor growth.
Building block for synthesis
Organic materials and pharmaceutical compounds 1H-Benz[f]indazole-4,9-dione has shown promise as a starting material for the synthesis of various organic materials and pharmaceutical compounds.
Unique chemical structure and versatile properties
Valuable for scientific and industrial applications The compound's distinctive structure and properties make it a valuable resource for a wide range of scientific and industrial uses.
Check Digit Verification of cas no
The CAS Registry Mumber 1015-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1015-97:
(6*1)+(5*0)+(4*1)+(3*5)+(2*9)+(1*7)=50
50 % 10 = 0
So 1015-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H6N2O2/c14-10-6-3-1-2-4-7(6)11(15)9-8(10)5-12-13-9/h1-5H,(H,12,13)
1015-97-0Relevant articles and documents
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Awad,Boulos
, p. 2665,2669 (1964)
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Synthesis of indazol-4,7-dione derivatives as potential trypanocidal agents
Tapia, Ricardo A.,Carrasco, Claudia,Ojeda, Scarlet,Salas, Cristian,Valderrama, Jaime A.,Morello, Antonio,Repetto, Yolanda
, p. 1093 - 1096 (2002)
The synthesis of new indazol-4,7-dione derivatives via 1,3-dipolar cycloaddition of diazomethane with 2,3-dimethyl-1,4-benzoquinone (2) and 1,4-naphthoquinone (7) followed by N-alkylation of the pyrazol nitrogen atom of the corresponding quinones (3) and (8) with methyl chloroacetate is described. A series of amides from esters (5) and (10) were also obtained. These compounds were tested in vitro as potential antitrypanosomal agents. Compounds (4) and (8) were found to have significant activity.
NEW METHODS AND REAGENTS IN ORGANIC SYNTHESIS. 87. REACTION OF TRIMETHYLSILYLDIAZOMETHANE WITH QUINONES
Aoyama, Toyohiko,Nakano, Takao,Nishigaki, Satoshi,Shioiri, Takayuki
, p. 375 - 379 (2007/10/02)
Reaction of trimethylsilyldiazomethane with various quinones affords indazoles 2, 2-substituted 3-trimethylsilylmethyl-1,4-quinones 3, silylcyclopropanes 4, and trimethylsilylmethylenedioxy derivatives 5, depending upon substrates.
