77603-15-7 Usage
Chemical structure
The compound has a complex structure that includes a pyrimidine ring fused to a quinoline ring.
Type of compound
It is a heterocyclic compound.
Usage
Often used in organic synthesis and medicinal chemistry.
Biological activities
Known to have biological activities and is being researched for its potential applications in pharmaceuticals.
Unique structure
Its unique structure makes it a useful building block in the synthesis of various organic compounds.
Diverse reactivity
Its diverse reactivity opens up possibilities for creating new drugs.
Importance in organic chemistry
The compound’s chemical properties and reactivity make it an important molecule in the field of organic chemistry and drug development.
Molecular weight
313.33 g/mol
Appearance
Yellow crystalline solid
Solubility
Soluble in organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO)
Melting point
The exact melting point is not provided in the material, but it is likely to have a high melting point due to its complex structure.
Stability
The compound is expected to be stable under normal conditions, but it may be sensitive to light, heat, and moisture.
Synthesis
The compound can be synthesized through various methods, such as condensation reactions, cyclization reactions, and other organic synthesis techniques.
Applications
Potential applications in pharmaceuticals, including the development of new drugs and drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 77603-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,0 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77603-15:
(7*7)+(6*7)+(5*6)+(4*0)+(3*3)+(2*1)+(1*5)=137
137 % 10 = 7
So 77603-15-7 is a valid CAS Registry Number.
77603-15-7Relevant academic research and scientific papers
Ring closure reactions of cyclic 2-arylaminomethylene-1,3-diones
Van Tinh, Dang,Fischer, Michaela,Stadlbauer, Wolfgang
, p. 905 - 910 (2007/10/03)
5-Arylaminomethylene compounds such as 5-arylaminomethylenepyrimidine-2,4,6-triones 2 or 2-phenylaminomethylenephenalene-1,3-dione 13 cyclize by thermolysis via migration of the arylamino group to pyrimido[4,5-b]quinoline-2,4-diones 6 or 7-oxo-7H-naphtho[
Reaction of Enaminones with Carbon Disulfide: Synthesis of Heterocycles Using Enamino Dithiocarboxylates
Tominaga, Yoshinori,Okuda, Hiroto,Mazume, Hisako
, p. 1245 - 1256 (2007/10/02)
Reaction of various types of enaminones, which are prepared by the condensation of 1,3-dicarbonyl compounds with aromatic amines, with carbon disulfide in the presence of sodium hydroxide as the base in dimethyl sulfoxide to give the corresponding enamino
A NEW SYNTHESIS OF PYRIMIDOQUINOLINE-2,4-(1H,3H)-DIONES BY REACTION OF 6-ARYLAMINO-1,3-DIMETHYLURACILS WITH CARBON DISULFIDE
Tominaga, Yoshinori,Okuda, Hiroto,Tochiki, Mutushi,Matsuda, Yoshiro,Kobayashi, Goro
, p. 679 - 683 (2007/10/02)
Reaction of 6-arylaminouracils (I) with carbon disulfide in the presence of sodium hydroxide and subsequent methylation with dimethyl sulfate gave the corresponding 1,3-dimethyl-5-methylthiopyrimidoquinoline-2,4(1H,3H)-diones (II).Raney-nickel desu