1033-34-7 Usage
Uses
Used in Pharmaceutical Industry:
6-Benzyl-2-(methylsulfanyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(1H)-one is used as a pharmaceutical compound for its potential biological activity. Its complex structure and the presence of various functional groups may contribute to its therapeutic effects, making it a valuable asset in the development of new drugs and treatments.
Used in Medicinal Chemistry Research:
6-Benzyl-2-(methylsulfanyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(1H)-one is used as a research compound in medicinal chemistry. Its unique structural features and potential biological activity make it an interesting subject for studying its interactions with biological targets and exploring its applications in drug discovery and development.
Used in Chemical Synthesis:
6-Benzyl-2-(methylsulfanyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(1H)-one is used as a building block in the synthesis of other chemical compounds. Its complex structure and functional groups can be utilized in various chemical reactions to create new molecules with specific properties and applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1033-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1033-34:
(6*1)+(5*0)+(4*3)+(3*3)+(2*3)+(1*4)=37
37 % 10 = 7
So 1033-34-7 is a valid CAS Registry Number.
1033-34-7Relevant academic research and scientific papers
2-Alkyl-4-oxohexahydropyrimido[4,5-d]- and -[5,4-d]azocines
Voskressensky,Ovcharov,Borisova,Kulikova,Listratova,Borisov,Varlamov
experimental part, p. 222 - 228 (2011/12/15)
It has been established that 2-R-4-oxotetrahydropyrido[4,3-d]pyrimidines, under the action of activated alkynes in methanol, form a mixture of 2-R-4-oxohexahydropyrimido[4,5-d]azocines and products of decomposition of the tetrahydropyridine ring, the 2-R-5-methoxymethyl-4-oxo-6-vinylaminoethyl- pyrimidines. Tetrahydropyrido[3,4-d]pyrimidine, isomeric at the junction of the pyrimidine and tetrahydropyridine rings, forms only the corresponding pyrimido[5,4-d]azocine, the product of expansion, under the action of methyl propiolate.
