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868654-38-0

5,10,15-tris(pentafluorophenyl)porphyrinatozinc(II) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 868654-38-0 Structure

  • Basic information

    1. Product Name: 5,10,15-tris(pentafluorophenyl)porphyrinatozinc(II)
    2. Synonyms: 5,10,15-tris(pentafluorophenyl)porphyrinatozinc(II)
    3. CAS NO:868654-38-0
    4. Molecular Formula:
    5. Molecular Weight: 871.882
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 868654-38-0.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: 5,10,15-tris(pentafluorophenyl)porphyrinatozinc(II)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,10,15-tris(pentafluorophenyl)porphyrinatozinc(II)(868654-38-0)
    11. EPA Substance Registry System: 5,10,15-tris(pentafluorophenyl)porphyrinatozinc(II)(868654-38-0)

  • 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: 868654-38-0(Hazardous Substances Data)

868654-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868654-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,5 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 868654-38:
(8*8)+(7*6)+(6*8)+(5*6)+(4*5)+(3*4)+(2*3)+(1*8)=230
230 % 10 = 0
So 868654-38-0 is a valid CAS Registry Number.

868654-38-0Relevant articles and documents

Enantiotopos-selective C-H oxygenation catalyzed by a supramolecular ruthenium complex

Frost, James R.,Huber, Stefan M.,Breitenlechner, Stefan,Bannwarth, Christoph,Bach, Thorsten

supporting information, p. 691 - 695 (2015/03/04)

Spirocyclic oxindoles undergo an enantioselective oxygenation reaction (nine examples; e.r. up to 97:3) upon catalysis by a chiral ruthenium porphyrin complex (1 mol%). The catalyst exhibits a lactam ring, which is responsible for substrate association through hydrogen bonds, and an active ruthenium center, which is in a defined spatial relationship to the oxygenation substrate. DFT calculations illustrate the perfect alignment of the active site with the reactive C-H bond and suggest-in line with the kinetic isotope effect-an oxygen rebound mechanism for the reaction.

Synthesis and cell phototoxicity of a triply bridged fused diporphyrin appended with six thioglucose units

Singh, Sunaina,Aggarwal, Amit,Bhupathiraju, N.V.S. Dinesh K.,Newton, Brandon,Nafees, Ahmad,Gao, Ruomei,Drain, Charles Michael

, p. 6311 - 6314 (2015/01/08)

A triply bridged fused diporphyrin appended with six thioglucose units is reported. This new, chemically, and photochemically stable amphiphilic compound is taken up by breast cancer cells and causes cell death upon light exposure. Photophysical studies r

METHODS AND COMPOSITIONS COMPRISING MACROCYCLES

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Page/Page column 10-11, (2011/06/26)

The present invention relates generally to methods and compositions comprising macrocycles. In some embodiments, the present invention provides methods for modifying macrocycles comprising a pendant group. In some cases, the pendent group comprises a hydrolyzable group. The present invention also provides methods for metallating a macrocycle using microwave energy, in some embodiments.

Efficient synthesis of hangman porphyrins

Dogutan, Dilek K.,Kwabena Bediako,Teets, Thomas S.,Schwalbe, Matthias,Nocera, Daniel G.

supporting information; experimental part, p. 1036 - 1039 (2010/06/15)

Chemical equation presented A two-step synthetic method has been designed to furnish hangman porphyrins In good yields from easily available starting materials. The use of the microwave Irradiation technique has been found to be valuable for delivering the car boxy lie acid hanging group in a much simplified and less time-consuming basic ester hydrolysis (4 h vs 7 days under harsh acidic conditions). The new route facilitates the synthesis of various hangman porphyrins that previously had limited or no access.

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