548475-67-8 Usage
Properties
1. Chemical Formula: C12H12N2O4
2. IUPAC Name: 1,7-dihydro-7-methoxy-1,3-dimethyl-2,4(3H)-dioxocyclohepta[c]furan
3. Molecular Weight: Approximately 244.23 g/mol
4. Molecular Structure: Contains a fused ring system consisting of a pyrimidine and a furan ring
5. Classification: Heterocyclic organic compound, derivative of furo[2,3-d]pyrimidine
6. Physical State: May exist as a solid or liquid depending on conditions such as temperature and pressure
7. Solubility: Solubility characteristics may vary depending on the specific solvent and conditions
8. Potential Biological Activities: May exhibit pharmacological properties due to its unique molecular structure
Specific Content
1. Fused Ring System: Contains a fused ring system comprising a pyrimidine ring and a furan ring, providing structural rigidity and potential for diverse interactions with biological targets.
2. Substituents: Features methyl groups (CH3) and a methoxy group (OCH3) at specific positions on the ring system, influencing its chemical and biological properties.
3. Functional Groups: Contains carbonyl groups (C=O) within the pyrimidine ring, which can participate in various chemical reactions and interactions.
4. Biological Activity: The compound's unique molecular structure and potential interactions with biological targets suggest possible pharmaceutical applications, although specific activities would require further research and analysis.
5. Medicinal Chemistry Potential: Its heterocyclic nature and potential pharmacological properties make it a candidate for further study in medicinal chemistry, including drug discovery and development.
6. Applications: While specific applications are not outlined, the compound's potential in pharmaceuticals hints at uses in areas such as drug design, therapeutic development, and biological research.
Overall, 2H-Cyclohepta[4,5]furo[2,3-d]pyrimidine-2,4(3H)-dione, 1,7-dihydro-7-methoxy-1,3-dimethyl(9CI) holds promise in medicinal chemistry and pharmaceuticals, with its unique molecular structure offering avenues for exploration in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 548475-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,4,7 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 548475-67:
(8*5)+(7*4)+(6*8)+(5*4)+(4*7)+(3*5)+(2*6)+(1*7)=198
198 % 10 = 8
So 548475-67-8 is a valid CAS Registry Number.
548475-67-8Relevant academic research and scientific papers
Novel synthesis and properties of 7,9-dimethylcyclohepta[b]pyrimido[5,4-d]furan-8(7H),10(9H)-dionylium tetrafluoroborate: Autorecycling oxidation of some alcohols under photo-irradiation
Naya, Shin-Ichi,Miyama, Hisashi,Yasu, Kenji,Takayasu, Tohru,Nitta, Makoto
, p. 1811 - 1821 (2007/10/03)
Three-step reactions starting from 2-chlorotropone with barbituric acid afforded novel 7,9-dimethylcyclohepta[b]pyrimido[5,4-d]furan-8(7H),10(9H)-dionylium tetrafluoroborate (9·BF4-), which is the isoelectronic compound of the 5-ethyl-3-methyllumiflavinium ion. The stability of cation 9 is expressed by the pKR+ value, which was determined spectrophotometrically, as ca. 6.0. The electrochemical reduction of 9 exhibited low reduction potential at -0.58 (V vs Ag/AgNO3), upon cyclic voltammetry (CV). In a search for the reactivity, reactions of 9·BF4- with some nucleophiles, hydroxide, hydride, amines, thiols, and methanol, were carried out to exhibit that the introduction of nucleophiles is dependent on the nucleophile itself. The photo-induced oxidation reactions of some alcohols catalyzed by 9·BF4- under aerobic conditions were carried out to give the corresponding carbonyl compounds in more than 100% yield [based on compound 9·BF4-], suggesting the oxidizing function of 9·BF4- toward alcohols in the autorecycling process. The UV-vis and fluorescence spectra of 9 were studied to suggest the electron transfer from alcohols to the excited 9.
