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1-[(2,6-difluorophenyl)methyl]-1H-1,2,3-triazole-4-carbonyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1020717-77-4 Structure
  • Basic information

    1. Product Name: 1-[(2,6-difluorophenyl)methyl]-1H-1,2,3-triazole-4-carbonyl chloride
    2. Synonyms: 1-[(2,6-difluorophenyl)methyl]-1H-1,2,3-triazole-4-carbonyl chloride
    3. CAS NO:1020717-77-4
    4. Molecular Formula:
    5. Molecular Weight: 257.627
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1020717-77-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-[(2,6-difluorophenyl)methyl]-1H-1,2,3-triazole-4-carbonyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[(2,6-difluorophenyl)methyl]-1H-1,2,3-triazole-4-carbonyl chloride(1020717-77-4)
    11. EPA Substance Registry System: 1-[(2,6-difluorophenyl)methyl]-1H-1,2,3-triazole-4-carbonyl chloride(1020717-77-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1020717-77-4(Hazardous Substances Data)

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

, 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.

SUBSTITUTED TRIAZOLES AND METHODS RELATING THERETO

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, (2016/08/23)

Substituted 1,2,3-triazole compounds are disclosed which have utility in the treatment of a variety of neurological disorders. The compounds provided herein have the general structure wherein R1, R2, R3 and n are as defined herein, including stereoisomers, esters, solvates and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound provided herein in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for treating neurological disorders in a subject in need thereof.

IMPROVED PROCESS FOR THE PREPARATION OF RUFINAMIDE

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, (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.

METHOD FOR THE PREPARATION OF RUFINAMIDE

-

Page/Page column 3, (2010/09/18)

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

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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