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1446713-83-2

13-bromo-1-(4-vinylphenyl)-2,5,8,11-tetraoxatridecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446713-83-2 Structure

  • Basic information

    1. Product Name: 13-bromo-1-(4-vinylphenyl)-2,5,8,11-tetraoxatridecane
    2. Synonyms: 13-bromo-1-(4-vinylphenyl)-2,5,8,11-tetraoxatridecane
    3. CAS NO:1446713-83-2
    4. Molecular Formula:
    5. Molecular Weight: 373.287
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446713-83-2.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: 13-bromo-1-(4-vinylphenyl)-2,5,8,11-tetraoxatridecane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 13-bromo-1-(4-vinylphenyl)-2,5,8,11-tetraoxatridecane(1446713-83-2)
    11. EPA Substance Registry System: 13-bromo-1-(4-vinylphenyl)-2,5,8,11-tetraoxatridecane(1446713-83-2)

  • 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: 1446713-83-2(Hazardous Substances Data)

1446713-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446713-83-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,7,1 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1446713-83:
(9*1)+(8*4)+(7*4)+(6*6)+(5*7)+(4*1)+(3*3)+(2*8)+(1*3)=172
172 % 10 = 2
So 1446713-83-2 is a valid CAS Registry Number.

1446713-83-2Downstream Products

1446713-83-2Relevant articles and documents

Copolymer-incarcerated nickel nanoparticles with N-heterocyclic carbene precursors as active cross-linking agents for Corriu-Kumada-Tamao reaction

Soule, Jean-Francois,Miyamura, Hiroyuki,Kobayashi, Shu

, p. 10602 - 10605 (2013)

We have developed heterogeneous polymer-incarcerated nickel nanoparticles (NPs), which catalyze cross-coupling reactions. The matrix structure of these catalysts incorporates both N-heterocyclic carbenes (NHCs) as ligands and Ni-NPs, thanks to a new design of cross-linking agents in polymer supports. These embedded NHCs were detected by field gradient swollen-resin magic angle spinning NMR analysis. They were successfully applied to Corriu-Kumada-Tamao reactions with a broad substrate scope including functional group tolerance, and the catalyst could be recovered and reused several times without loss of activity.

N-heterocyclic carbene coordinated heterogeneous Pd nanoparticles as catalysts for suzuki-miyaura coupling

Min, Hyemin,Miyamura, Hiroyuki,Kobayashi, Shu

supporting information, p. 837 - 839 (2016/07/16)

Palladium nanoparticle (Pd NP) catalysts immobilized in a polymer with an N-heterocyclic carbene (NHC) moiety (PICBNHC-Pd) have been developed, wherein the NHC moiety plays dual roles as a crosslinker and a ligand to activate the Pd NPs. The presence of both Pd NPs and NHC was confirmed by STEM/EDS and SR-MAS NMR analyses, respectively. This PICB-NHC-Pd catalyst showed excellent activity in the Suzuki-Miyaura coupling reaction without leaching of Pd. Excellent results were obtained in gram-scale synthesis, and catalyst recovery/reuse experiments were completed without loss of catalyst activity.

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