81549-28-2 Usage
Uses
Used in Pharmaceutical Industry:
(6Z)-2-phenyl-7a,8,8a,9-tetrahydro-1H,5H-5,9-ethenocyclopropa[d][1,2,4]triazolo[1,2-a][1,2]diazocine-1,3(2H)-dione is used as a potential therapeutic agent for various medical conditions due to its pharmacological attributes and potential range of biological activities. Its unique chemical structure and properties make it an interesting target for the development of new drugs and treatments.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (6Z)-2-phenyl-7a,8,8a,9-tetrahydro-1H,5H-5,9-ethenocyclopropa[d][1,2,4]triazolo[1,2-a][1,2]diazocine-1,3(2H)-dione serves as a subject of study for understanding its chemical properties, interactions with biological systems, and potential applications in the design of new pharmaceuticals.
Used in Drug Development:
(6Z)-2-phenyl-7a,8,8a,9-tetrahydro-1H,5H-5,9-ethenocyclopropa[d][1,2,4]triazolo[1,2-a][1,2]diazocine-1,3(2H)-dione is utilized in drug development as a starting point for the creation of new compounds with improved pharmacological properties. Its unique structure and potential biological activities make it a valuable asset in the search for novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 81549-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,4 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81549-28:
(7*8)+(6*1)+(5*5)+(4*4)+(3*9)+(2*2)+(1*8)=142
142 % 10 = 2
So 81549-28-2 is a valid CAS Registry Number.
81549-28-2Relevant academic research and scientific papers
-Cycloaddition of Singlet Oxygen and Phenyltriazolinedione with Bicyclonona-2,4,6-triene and Derivatives
Adam, Waldemar,Cueto, Omar,Lucchi, Ottorino De
, p. 1170 - 1177 (2007/10/02)
The dienic reactivity of the bicyclononatrienes 1a (-isomer) and 1b (-isomer) and its oxa-derivative 6 (cyclooctatetraene epoxide) as well as 1,3,5-cyclooctatrienone (7), towards singlet oxygen (1O2) and phenyl-1,2,4-triazoline-3,5-dione (PTAD) as dienophiles has been investigated.Except for 1a, which affords the endoperoxide 9a in 60percent yield, the remaining substrates 1b, 6, and 7 do not react with 1O2.With PTAD 1a, 1b, 6, and 7 afford the urazoles 10a, 8b, 12c, and 11, respectively.Unusual is the fact that the bicyclotriene 1b leads only to the tri cyclic urazole 8b, the first example of this type of -cycloadduct of 1b, while the oxa-analog 6 affords only the tetracyclic urazole 12c.Moreover, 6 reacts with PTAD considerably more sluggishly than 1b.
