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bis[(5-hexyl-10,20-diphenylporphyrin-15-ylato)zinc(II)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1314641-97-8 Structure
  • Basic information

    1. Product Name: bis[(5-hexyl-10,20-diphenylporphyrin-15-ylato)zinc(II)]
    2. Synonyms: bis[(5-hexyl-10,20-diphenylporphyrin-15-ylato)zinc(II)]
    3. CAS NO:1314641-97-8
    4. Molecular Formula:
    5. Molecular Weight: 1218.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1314641-97-8.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: bis[(5-hexyl-10,20-diphenylporphyrin-15-ylato)zinc(II)](CAS DataBase Reference)
    10. NIST Chemistry Reference: bis[(5-hexyl-10,20-diphenylporphyrin-15-ylato)zinc(II)](1314641-97-8)
    11. EPA Substance Registry System: bis[(5-hexyl-10,20-diphenylporphyrin-15-ylato)zinc(II)](1314641-97-8)
  • 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: 1314641-97-8(Hazardous Substances Data)

1314641-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1314641-97-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,6,4 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1314641-97:
(9*1)+(8*3)+(7*1)+(6*4)+(5*6)+(4*4)+(3*1)+(2*9)+(1*7)=138
138 % 10 = 8
So 1314641-97-8 is a valid CAS Registry Number.

1314641-97-8Downstream Products

1314641-97-8Relevant articles and documents

Synthesis and functionalization of triply fused porphyrin dimers

Ryan, Aoife A.,Senge, Mathias O.

, p. 3700 - 3711 (2013/07/19)

Current applications of porphyrins in medicine and optics, such as photodynamic therapy or nonlinear absorption, increasingly require the use of far-red absorbing dyes. Modification of the porphyrin structure to accommodate these conditions can be achieved by extending the conjugation of the porphyrin π system, which causes a bathochromic shift in the absorption spectrum. Thus, conjugated porphyrin oligomers have found widespread use. However, past synthetic strategies have mainly targeted symmetric porphyrin dimers, trimers, and oligomers which limit the practical use of such chromophores. To further extend the absorption profile, a series of symmetric and unsymmetric dimeric and oligomeric porphyrin β-β, meso-meso, β′-β′ triply fused systems were synthesized by oxidative coupling methods. This required an analysis and optimization of the various synthetic strategies. These arrays exhibit a dramatic bathochromic shift into the near-infrared region and many display absorption at wavelengths greater than 1050 nm. Additionally, post-fusing chemical transformations, namely, organolithium, cycloaddition, and transition-metal-catalyzed reactions, at the meso and β positions enable the fine-tuning of such arrays to enhance the bathochromic shift and their potential optical applications. A library of symmetric and unsymmetric singly linked and triply fused porphyrin dimers are synthesized in moderate to very good yields. A variety of functional groups are tolerated. Numerous synthetic strategies, incorporating oxidative radical coupling and organolithium and palladium-catalyzed coupling methods, are utilized. Copyright

Synthesis and crystal structure of a meso-meso directly linked bisporphyrin

Senge, Mathias O.,Pintea, Monica,Ryan, Aoife A.

, p. 553 - 558 (2011/08/08)

We report the synthesis and characterization of a meso-meso directly linked bisporphyrin 6 bearing both alkyl and aryl residues. Its oxidative fusing results in the corresponding meso-meso β-β,β-β- linked bisporphyrin. The first crystal structure analysis

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