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1-(2-(2-(4-bromophenoxy)ethoxy)ethyl)-4-phenyl-1H-1,2,3-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1361031-85-7 Structure
  • Basic information

    1. Product Name: 1-(2-(2-(4-bromophenoxy)ethoxy)ethyl)-4-phenyl-1H-1,2,3-triazole
    2. Synonyms: 1-(2-(2-(4-bromophenoxy)ethoxy)ethyl)-4-phenyl-1H-1,2,3-triazole
    3. CAS NO:1361031-85-7
    4. Molecular Formula:
    5. Molecular Weight: 388.264
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1361031-85-7.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-(2-(4-bromophenoxy)ethoxy)ethyl)-4-phenyl-1H-1,2,3-triazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-(2-(4-bromophenoxy)ethoxy)ethyl)-4-phenyl-1H-1,2,3-triazole(1361031-85-7)
    11. EPA Substance Registry System: 1-(2-(2-(4-bromophenoxy)ethoxy)ethyl)-4-phenyl-1H-1,2,3-triazole(1361031-85-7)
  • 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: 1361031-85-7(Hazardous Substances Data)

1361031-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1361031-85-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,0,3 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1361031-85:
(9*1)+(8*3)+(7*6)+(6*1)+(5*0)+(4*3)+(3*1)+(2*8)+(1*5)=117
117 % 10 = 7
So 1361031-85-7 is a valid CAS Registry Number.

1361031-85-7Downstream Products

1361031-85-7Relevant articles and documents

A photoreducible copper(ii)-tren complex of practical value: Generation of a highly reactive click catalyst

Harmand, Lydie,Lambert, Romain,Scarpantonio, Luca,McClenaghan, Nathan D.,Lastecoueres, Dominique,Vincent, Jean-Marc

, p. 16231 - 16239 (2013)

A detailed study on the photoreduction of the copper(II) precatalyst 1 to generate a highly reactive cuprous species for the copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) click reaction is presented. For the photoactive catalyst described herein, the activation is driven by a photoinduced electron transfer (PET) process harnessing a benzophenone-like ketoprofenate chromophore as a photosensitizer, which is equally the counterion. The solvent is shown to play a major role in the CuII to Cu I reduction process as the final electron source, and the influence of the solvent nature on the photoreduction efficiency has been studied. Particular attention was paid to the use of water as a potential solvent, aqueous media being particularly appealing for CuAAC processes. The ability to solubilize the copper-tren complexes in water through the formation of inclusion complexes with β-CDs is demonstrated. Data is also provided on the fate of the copper(I)-tren catalytic species when reacting with O2, O 2 being used to switch off the catalysis. These data show that partial oxidation of the secondary benzylamine groups of the ligand to benzylimines occurs. Preliminary results show that when prolonged irradiation times are employed a CuI to Cu0 over-reduction process takes place, leading to the formation of copper nanoparticles (NPs). Finally, the main objective of this work being the development of photoactivable catalysts of practical value for the CuAAC, the catalytic, photolatent, and recycling properties of 1 in water and organic solvents are reported. Copyright

Huisgen click cycloadditions from a copper(II)-tren precatalyst without external sacrificial reductant

Harmand, Lydie,Lescure, Marie-Hélne,Candelon, Nicolas,Duttine, Mathieu,Lastécoures, Dominique,Vincent, Jean-Marc

experimental part, p. 1417 - 1420 (2012/03/27)

The copper(II) complex [Cu(C186tren)](Br)2, 2, is an efficient precatalyst for the Huisgen 'click' cycloaddtion which can be used at low loading without the requirement of an external sacrificial reductant such as sodium ascorbate. E

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