55259-87-5 Usage
Molecular structure
1-phenyl-6,7,8,9-tetrahydro-5H-[1]benzothieno[3,2-e][1,3]thiazolo[3,2-a]pyrimidin-5-one consists of a phenyl group, a fused benzothieno and thiazolo ring system, and a pyrimidin-5-one moiety.
Complexity
The compound has a complex and specific structure, which may contribute to its potential pharmaceutical or biological applications.
Phenyl group
The presence of a phenyl group (a carbon-based ring with delocalized electrons) may contribute to the compound's stability and chemical properties.
Fused rings
The benzothieno and thiazolo rings are fused together, creating a unique and stable structure.
Pyrimidin-5-one moiety
The presence of a pyrimidin-5-one group (a nitrogen-containing ring with an oxygen atom) may contribute to the compound's potential biological activity.
Potential applications
Due to its unique structure, 1-phenyl-6,7,8,9-tetrahydro-5H-[1]benzothieno[3,2-e][1,3]thiazolo[3,2-a]pyrimidin-5-one may have potential pharmaceutical or biological applications.
Further research needed
The exact properties and uses of 1-phenyl-6,7,8,9-tetrahydro-5H-[1]benzothieno[3,2-e][1,3]thiazolo[3,2-a]pyrimidin-5-one would need to be determined through additional research and testing to fully understand its potential applications and behavior.
Check Digit Verification of cas no
The CAS Registry Mumber 55259-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,5 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55259-87:
(7*5)+(6*5)+(5*2)+(4*5)+(3*9)+(2*8)+(1*7)=145
145 % 10 = 5
So 55259-87-5 is a valid CAS Registry Number.
55259-87-5Relevant academic research and scientific papers
Synthesis of 1-Aryl-6,7,8,9-tetrahydrobenzothienothiazolopyrimidin-5(H)-ones
Gakhar, H. K.,Madan, Arun,Kumar, Naresh
, p. 250 - 252 (2007/10/02)
1-Aryl-6,7,8,9-tetrahydrobenzothienothiazolopyrimidin-5(H)-ones (IIa-e) have been synthesised by the condensation of ethyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate with α-thiocyanoacetophenones.Various intermediates have been isolated and their structures established on the basis of IR and PMR data.The course of reaction has also been rationalized.