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1-{2-[(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methoxy]ethyl}triaza-1,2-dien-2-ium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80504-58-1

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80504-58-1 Usage

Chemical structure

A complex structure containing a triaza-dien-2-ium group, a methoxyethyl group, and a dioxo-dihydropyrimidin-yl moiety.

Potential biological activity

Due to its unique structure, it may have potential biological activity.

Pharmaceutical research interest

It could be of interest in pharmaceutical research for the development of new drugs.

Further study needed

Further study and analysis are required to fully understand the properties and potential applications of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 80504-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,0 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80504-58:
(7*8)+(6*0)+(5*5)+(4*0)+(3*4)+(2*5)+(1*8)=111
111 % 10 = 1
So 80504-58-1 is a valid CAS Registry Number.

80504-58-1Downstream Products

80504-58-1Relevant academic research and scientific papers

Design, modeling & synthesis of 1,2,3-triazole-linked nucleoside-amino acid conjugates as potential antibacterial agents

Malkowski, Sarah N.,Dishuck, Carolyn F.,Lamanilao, Gene G.,Embry, Carter P.,Grubb, Christopher S.,Cafiero, Mauricio,Peterson, Larryn W.

, (2017/11/07)

Copper-catalyzed azide-alkyne cycloadditions (CuAAC or click chemistry) are convenient methods to easily couple various pharmacophores or bioactive molecules. A new series of 1,2,3- Triazole-linked nucleoside-amino acid conjugates have been designed and synthesized in 57-76% yields using CuAAC. The azido group was introduced on the 50-position of uridine or the acyclic analogue using the tosyl-azide exchange method and alkylated serine or proparylglycine was the alkyne. Modeling studies of the conjugates in the active site of LpxC indicate they have promise as antibacterial agents.

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