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1H-[1,2,4]Triazolo[1,2-a]pyridazine-1,3(2H)-dione, 5,8-dihydro-2-phenyl- is a complex organic compound with the molecular formula C10H7N5O2. It features a triazolo[1,2-a]pyridazine core, which is a fused ring system consisting of a triazole and a pyridazine. The compound is characterized by a 5,8-dihydro substitution, indicating the presence of two hydrogen atoms attached to the 5th and 8th positions of the molecule, and a 2-phenyl group, which is a phenyl ring attached to the 2nd position. This chemical structure contributes to its unique properties and potential applications in various fields, such as pharmaceuticals or materials science.

15971-64-9

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15971-64-9 Usage

Type of Compound

Heterocyclic compound

Structure

Contains a triazolo-pyridazine ring and a phenyl group

Potential Applications

Medicinal chemistry, as a potential drug candidate or chemical building block for synthesizing other biologically active molecules

Pharmacological Activities

Not well-documented

Safety Measures

Proper safety measures and protocols should be followed when handling and using 1H-[1,2,4]Triazolo[1,2-a]pyridazine-1,3(2H)-dione, 5,8-dihydro-2-phenyl-

Check Digit Verification of cas no

The CAS Registry Mumber 15971-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,7 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15971-64:
(7*1)+(6*5)+(5*9)+(4*7)+(3*1)+(2*6)+(1*4)=129
129 % 10 = 9
So 15971-64-9 is a valid CAS Registry Number.

15971-64-9Relevant academic research and scientific papers

Thermal ring opening of 1,1-dibromo and 1-bromo-2- chloromethylcyclopropanes: Observation of a formal debromochlorination

Sydnes, Leiv K.,Alnes, Karl F. S.,Pettersen, Anita,Brinker, Udo H.

experimental part, p. 479 - 483 (2010/06/16)

When the title compounds are thermolyzed in the gas phase under vacuum or in hot quinoline, several products are formed. A predominant product in all cases is a chlorine-free buta-1,3-diene which has been formed by formal debromochlorination, a reaction n

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