1161004-77-8 Usage
Chemical class
Heterocyclic compound
Explanation
It contains a ring structure with both carbon and non-carbon atoms, specifically nitrogen in this case.
Explanation
A derivative of pyridazinone, which is a heterocyclic compound with a core structure of a five-membered ring containing four carbon atoms and one nitrogen atom.
Explanation
The presence of a trifluoromethyl (CF3) group and a methoxyphenyl (ArOCH3) group contributes to the compound's unique chemical and pharmacological properties.
Explanation
The compound may exhibit various biological activities, making it a potential candidate for drug development in treating inflammation, pain, or cell proliferation-related diseases.
Explanation
The specific arrangement of carbon, nitrogen, and the functional groups mentioned above make this compound a subject of interest for medicinal and pharmaceutical research.
Derivative
Pyridazinone derivative
Functional groups
Trifluoromethyl group and methoxyphenyl group
Potential pharmaceutical applications
Anti-inflammatory, analgesic, or antiproliferative effects
Structural features
Unique arrangement of atoms and functional groups
Check Digit Verification of cas no
The CAS Registry Mumber 1161004-77-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,1,0,0 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1161004-77:
(9*1)+(8*1)+(7*6)+(6*1)+(5*0)+(4*0)+(3*4)+(2*7)+(1*7)=98
98 % 10 = 8
So 1161004-77-8 is a valid CAS Registry Number.
1161004-77-8Relevant articles and documents
Concise synthesis of ω-fluoroalkylated ketoesters. A building block for the synthesis of six-, seven-, and eight-membered fluoroalkyl substituted 1,2-diaza-3-one heterocycles
Wan, Wen,Hou, Jie,Jiang, Haizhen,Wang, Yangli,Zhu, Shizheng,Deng, Hongmei,Hao, Jian
experimental part, p. 4212 - 4219 (2009/09/30)
A concise and general synthetic route toward the small and medium-sized fluoroalkyl substituted 1,2-diaza-3-one heterocyclic ring skeletons via a sequential reaction of condensation and ring-closure reaction of ω-fluoroalkylated ketoesters 4 with hydrazin