69579-13-1 Usage
Chemical structure
Hydrazine derivative with a morpholine ring and a pyridazine ring
The compound has a hydrazine functional group, which is connected to a morpholine ring and a pyridazine ring.
Tert-butoxycarbonyl-protected propylidene group
The compound features a tert-butoxycarbonyl (t-Boc) group, which is a protecting group for the propylidene moiety.
Medicinal chemistry research
Potential drug candidate
The compound is often used in medicinal chemistry research due to its hydrazine moiety, which has been found to exhibit various biological activities.
Applications
Organic synthesis and chemical research
The compound may have applications in the field of organic synthesis and chemical research, likely due to its unique structure and functional groups.
Biological activities
Exhibited by the hydrazine moiety
The hydrazine functional group in the compound is responsible for its various biological activities, making it a valuable compound for research and potential drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 69579-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,7 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69579-13:
(7*6)+(6*9)+(5*5)+(4*7)+(3*9)+(2*1)+(1*3)=181
181 % 10 = 1
So 69579-13-1 is a valid CAS Registry Number.
69579-13-1Relevant articles and documents
Synthesis and antihypertensive activity of novel 6-substituted-3-pyridazinylhydrazones
Szilagyi,Kasztreiner,Matyus,et al.
, p. 111 - 117 (2007/10/02)
The synthesis and hypotensive properties of a series of 6-substituted-3-pyridazinylhydrazones are described. The most active compound of the series. 1-(6-morpholino-3-pyridazinyl)-2-[1-(tert-butoxycarbonyl)-2-propylidene] hydrazine, is a more potent hypotensive agent than hydralazine with a longer duration of action and a lower toxicity. Structure-activity relationships are discussed.