95095-69-5 Usage
Phenyl group
A benzene ring, which is an aromatic ring with delocalized electrons, attached to an ethanone moiety.
Ethanone moiety
A two-carbon chain with a ketone group (C=O) at one end.
Amino group
A nitrogen atom with two hydrogen atoms attached, connected to the triazole ring.
Organic synthesis
APT is used as a building block for the synthesis of potential drugs and other organic compounds.
Pharmaceutical research
It is used in the development of new drugs due to its diverse chemical properties.
Coordination chemistry
APT can form complexes with metal ions, which exhibit biological activities.
Antifungal
The compound can inhibit the growth of fungi.
Antibacterial
It can stop the growth and reproduction of bacteria.
Antiviral
APT can prevent the replication and spread of viruses.
Reagent use
APT is used as a reagent in organic reactions, such as nucleophilic substitution and Mannich-type reactions, due to its reactive functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 95095-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,9 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95095-69:
(7*9)+(6*5)+(5*0)+(4*9)+(3*5)+(2*6)+(1*9)=165
165 % 10 = 5
So 95095-69-5 is a valid CAS Registry Number.
95095-69-5Relevant academic research and scientific papers
Applications of alkaloid essramycin and derivative thereof in resisting of plant viruses
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Paragraph 0021-0026, (2020/01/30)
The invention relates to applications of alkaloid essramycin and a derivative thereof in resisting of plant viruses, wherein the chemical structural formula of the alkaloid essramycin is represented in the specification, specifically the alkaloid essramyc
Synthesis of essramycin and comparison of its antibacterial activity
Tee, Ernest H. L.,Karoli, Tomislav,Ramu, Soumya,Huang, Johnny X.,Butler, Mark S.,Cooper, Matthew A.
experimental part, p. 1940 - 1942 (2011/02/28)
The triazolopyrimidine natural product essramycin (1) was synthesized without the use of protecting groups via a two-step reaction scheme involving a 3-amino-1,2,4-triazole intermediate, and its structure was unequivocally determined. However, in contrast
A short synthesis of the triazolopyrimidine antibiotic essramycin
Battaglia, Ugo,Moody, Christopher J.
experimental part, p. 1938 - 1939 (2011/02/26)
A short synthesis of the 1,2,4-triazolo[1,5-a]pyrimidine antibiotic essramycin is described involving condensation of aminoguanidine with ethyl benzoylacetate to give an amino-1,2,4-triazole, followed by condensation with ethyl acetoacetate to form the py
