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2-[1,2,4]triazolo[4,3-a]quinolin-1-yl-phenol is a complex organic compound with the molecular formula C13H8N4O. It is characterized by a phenol group attached to a triazoloquinoline ring system. 2-[1,2,4]triazolo[4,3-a]quinolin-1-yl-phenol is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active molecules. The triazoloquinoline structure is of interest due to its presence in certain antitumor and antiviral agents, suggesting that 2-[1,2,4]triazolo[4,3-a]quinolin-1-yl-phenol may have similar properties. Its synthesis and biological evaluation are areas of ongoing research, with the aim of discovering new therapeutic agents.

2839-84-1

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2839-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2839-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,3 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2839-84:
(6*2)+(5*8)+(4*3)+(3*9)+(2*8)+(1*4)=111
111 % 10 = 1
So 2839-84-1 is a valid CAS Registry Number.

2839-84-1Downstream Products

2839-84-1Relevant academic research and scientific papers

STUDIES ON THIOAMIDES AND THEIR DERIVATIVES. PART II. REACTION OF QUATERNARY SALTS OF N,N-DISUBSTITUTED THIOAMIDES WITH 2-HYDRAZINOQUINOLINE

Santus, Maria

, p. 661 - 671 (2007/10/02)

In reactions of methyliodides of N,N-disubstituted thioamides with 2-hydrazinoquinoline a series of new compounds have been obtained: iodohydrides, derivatives of 1-α-morpholinobenzylidene-2-quinolinohydrazine and of 1-α-piperidinobenzylidene-2-quinolinohydrazine.The compounds obtained, when transformed into free bases, undergo cyclization to derivatives of s-triazolo(4,3-a)quinoline system under the effect of glacial acetic acid.All these compounds have been characterized by means of UV and IR spectra.

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