55610-02-1 Usage
Description
1,2-Dimethoxy-6-methyl-4H-dibenzo[de,g]quinoline-4,5(6H)-dione is a further aporphine type alkaloid derived from the callus tissue of Stephania cepharantha. This alkaloid is the dimethoxy analogue of the preceding base and forms orange needles, exhibiting bright orange fluorescence. Its ultraviolet spectrum in ethanol has absorption maxima at 213, 244, 303, 315, and 440 nm, with a shoulder at 273 nm.
Uses
Used in Pharmaceutical Industry:
1,2-Dimethoxy-6-methyl-4H-dibenzo[de,g]quinoline-4,5(6H)-dione is used as a pharmaceutical compound for its potential therapeutic applications. The alkaloid's unique chemical structure and fluorescent properties make it a promising candidate for the development of new drugs and therapies.
Used in Research and Development:
In the field of research and development, 1,2-Dimethoxy-6-methyl-4H-dibenzo[de,g]quinoline-4,5(6H)-dione serves as a valuable compound for studying its chemical properties, potential interactions with biological systems, and possible applications in various industries, including pharmaceuticals, agriculture, and materials science.
Used in Analytical Chemistry:
The bright orange fluorescence and distinct ultraviolet absorption spectrum of 1,2-Dimethoxy-6-methyl-4H-dibenzo[de,g]quinoline-4,5(6H)-dione make it a useful compound in analytical chemistry for the development of new methods and techniques for detecting and analyzing similar compounds.
Used in Material Science:
The unique properties of 1,2-Dimethoxy-6-methyl-4H-dibenzo[de,g]quinoline-4,5(6H)-dione, such as its fluorescence and absorption characteristics, may also find applications in material science, where it could be used in the development of new materials with specific optical, electronic, or sensing properties.
Check Digit Verification of cas no
The CAS Registry Mumber 55610-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,1 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55610-02:
(7*5)+(6*5)+(5*6)+(4*1)+(3*0)+(2*0)+(1*2)=101
101 % 10 = 1
So 55610-02-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H15NO4/c1-20-13-8-10-6-4-5-7-11(10)16-15(13)12(17(21)19(20)22)9-14(23-2)18(16)24-3/h4-9H,1-3H3
55610-02-1Relevant articles and documents
A versatile approach to the synthesis of 4,5-dioxoaporphine and 3,4-dioxocularine alkaloids. One-pot sequential C/B ring formation from arylacetamides
Suau, Rafael,Lopez-Romero, Juan Manuel,Rico, Rodrigo
, p. 9357 - 9360 (1996)
Cyclization of biarylacetamides to their phenanthrene derivatives is promoted by oxalyl chloride/stannyl chloride. The reaction proceeds with a second cyclization in which the oxalyl fragment acts as an α-dicarbonyl transfer agent to give 4,5-dioxoaporphine alkaloids in a single step. This double cyclization was also applied to an aryloxyphenyl acetamides to give the corresponding 3,4-dioxocularine alkaloids. Decarbonylated aristocularine alkaloids were also formed in this case.
Synthesis and biological evaluation of cepharadiones A and B and related dioxoaporphines
Elban, Mark A.,Chapuis, Jean C.,Li, Mei,Hecht, Sidney M.
, p. 6119 - 6125 (2008/03/28)
Described herein is the first total synthesis and structural confirmation of cepharadione A, a naturally occurring DNA damaging agent. Also reported is the synthesis of cepharadione B, a closely related natural product, as well as the biological evaluatio
Sequential bicyclization of biphenyl acetamides promoted by (COCl)2/SnCl4. Total synthesis of 4,5-dioxoaporphines
Suau, Rafael,Lopez-Romero, Juan Manuel,Rico, Rodrigo
, p. 14397 - 14410 (2007/10/03)
The reaction of biphenyl acetamides with excess of oxalyl chloride/stannyl chloride offers a one pot, high-yield entry to 4,5-dioxoaporphine alkaloids. This strategy has been applied to the synthesis of 4,5-dioxodehydrocorydine starting from 1-iodo-2,3-dimethoxybenzene. The cytotoxicity of tetraoxygenated 4,5-dioxoaporphines has been evaluated.
