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1020717-77-4

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1020717-77-4 Usage

Chemical class

Triazole derivatives

Functional group

Carbonyl chloride

Structure

1-[(2,6-difluorophenyl)methyl]-1H-1,2,3-triazole-4-carbonyl group attached

Potential applications

Synthesis of biologically active compounds, pharmaceutical industry, medicinal chemistry, development of new drugs and therapeutic agents

Handling precautions

Potential reactivity and toxicity, handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 1020717-77-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,7,1 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1020717-77:
(9*1)+(8*0)+(7*2)+(6*0)+(5*7)+(4*1)+(3*7)+(2*7)+(1*7)=104
104 % 10 = 4
So 1020717-77-4 is a valid CAS Registry Number.

1020717-77-4Downstream Products

1020717-77-4Relevant articles and documents

Derisking the Cu-Mediated 18F-Fluorination of Heterocyclic Positron Emission Tomography Radioligands

Taylor, Nicholas J.,Emer, Enrico,Preshlock, Sean,Schedler, Michael,Tredwell, Matthew,Verhoog, Stefan,Mercier, Joel,Genicot, Christophe,Gouverneur, Véronique

supporting information, p. 8267 - 8276 (2017/06/27)

Molecules labeled with fluorine-18 (18F) are used in positron emission tomography to visualize, characterize and measure biological processes in the body. Despite recent advances in the incorporation of 18F onto arenes, the development of general and efficient approaches to label radioligands necessary for drug discovery programs remains a significant task. This full account describes a derisking approach toward the radiosynthesis of heterocyclic positron emission tomography (PET) radioligands using the copper-mediated 18F-fluorination of aryl boron reagents with 18F-fluoride as a model reaction. This approach is based on a study examining how the presence of heterocycles commonly used in drug development affects the efficiency of 18F-fluorination for a representative aryl boron reagent, and on the labeling of more than 50 (hetero)aryl boronic esters. This set of data allows for the application of this derisking strategy to the successful radiosynthesis of seven structurally complex pharmaceutically relevant heterocycle-containing molecules.

IMPROVED PROCESS FOR THE PREPARATION OF RUFINAMIDE

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Page/Page column 10, (2012/03/26)

The invention relates to a novel, industrially viable, cost effective process for the preparation of 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxamide commonly known as Rufinamide and intermediates thereof.

Process for the preparation of rufinamide

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Page/Page column 6, (2010/10/03)

The invention provides a novel process for the regioselective preparation of a compound of formula (I)

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