219715-67-0 Usage
Uses
Used in Pharmaceutical Development:
[1,2,4]Triazolo[1,5-c]pyrimidin-2-amine,8-ethoxy-5-methoxy-(9CI) is used as a potential candidate in the development of pharmaceutical drugs due to its unique molecular structure and chemical properties. The presence of nitrogen atoms in the triazolo and pyrimidin rings may allow for interactions with specific biological targets, potentially leading to the creation of novel therapeutic agents.
Used in Medicinal Chemistry Research:
[1,2,4]Triazolo[1,5-c]pyrimidin-2-amine,8-ethoxy-5-methoxy-(9CI) is also used as a research tool in medicinal chemistry, where its unique properties can be explored for various applications. The ethoxy and methoxy side chains, along with the triazolo and pyrimidin rings, may provide valuable insights into the design and synthesis of new chemical entities with potential therapeutic benefits.
Used in Biological Studies:
[1,2,4]Triazolo[1,5-c]pyrimidin-2-amine,8-ethoxy-5-methoxy-(9CI) may be employed in biological studies to investigate its interactions with various biological systems. [1,2,4]Triazolo[1,5-c]pyrimidin-2-amine,8-ethoxy-5-methoxy-(9CI)'s unique structure could provide valuable information on its potential role in biological processes and its effects on cellular functions, which may contribute to the understanding of its possible applications in medicine and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 219715-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,7,1 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 219715-67:
(8*2)+(7*1)+(6*9)+(5*7)+(4*1)+(3*5)+(2*6)+(1*7)=150
150 % 10 = 0
So 219715-67-0 is a valid CAS Registry Number.
219715-67-0Relevant academic research and scientific papers
Penoxsulam-Structure-activity relationships of triazolopyrimidine sulfonamides
Johnson, Timothy C.,Martin, Timothy P.,Mann, Richard K.,Pobanz, Mark A.
experimental part, p. 4230 - 4240 (2009/10/02)
The discovery of the sulfonamide herbicides, which inhibit the enzyme acetolactate synthase (ALS), has resulted in many investigations to exploit their herbicidal activity. One area which proved particularly productive was the N-aryltriazolo[1,5-c]pyrimidine sulfonamides, providing three commercial herbicides, cloransulam-methyl, diclosulam and florasulam. Additional structure-activity investigations by reversing the sulfonamide linkage resulted in the discovery of triazolopyrimidine sulfonamides with cereal crop selectivity and high levels of grass and broadleaf weed control. Research efforts to exploit these high levels of weed activity ultimately led to the discovery of penoxsulam, a new herbicide developed for grass, sedge and broadleaf weed control in rice. Synthetic efforts and structure-activity relationships leading to the discovery of penoxsulam will be discussed.
