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C70H64N4O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 360076-32-0 Structure
  • Basic information

    1. Product Name: C70H64N4O2
    2. Synonyms: C70H64N4O2
    3. CAS NO:360076-32-0
    4. Molecular Formula:
    5. Molecular Weight: 993.304
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 360076-32-0.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: C70H64N4O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C70H64N4O2(360076-32-0)
    11. EPA Substance Registry System: C70H64N4O2(360076-32-0)
  • 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: 360076-32-0(Hazardous Substances Data)

360076-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 360076-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,0,0,7 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 360076-32:
(8*3)+(7*6)+(6*0)+(5*0)+(4*7)+(3*6)+(2*3)+(1*2)=120
120 % 10 = 0
So 360076-32-0 is a valid CAS Registry Number.

360076-32-0Downstream Products

360076-32-0Relevant articles and documents

New methodologies for the preparation of porphodimethenes and their conversion to trans-porphyrins with functionalized naphthyl spacers

Harmjanz,Gill,Scott

, p. 5374 - 5383 (2001)

The MacDonald [2 + 2]-type condensation of readily available 5-aryl-substituted dipyrromethanes with acenaphthenequinone leads to the trans-syn- and anti-porphodimethenes, which in turn can be converted to the α,α- and α,β-porphyrin atropisomers, respectively. Treatment of the metalated or unmetalated porphodimethenes with KOH or NaOMe in THF followed by protonation with HCl results in a ring opening of the acenaphthenone and formation of the trans-8-carboxynaphthylporphyrins or their esters (NaOMe) after oxidation. Alternatively, the porphyrin formation can be accomplished by reaction of the porphodimethenes with acids in the presence of water or methanol. Reaction with NaBH4 in a THF-methanol mixture yields the corresponding dialcohols in nearly quantitative yields. Sixteen different building blocks were prepared in order to evaluate the generality of this new synthetic approach, with Ar = 2,4,6-Me3C6H2; 2,6-Cl2C6H3; 2,6-F2C6H3; 3,4-tBu2C6H3; 3,4,5-(MeO)3C6H2; 4-BrC6H4; 4-MeC6H4; and 4-MeOOCC6H4 at the meso positions. The synthesized porphodimethenes and porphyrins have been fully characterized, and the X-ray structure analyses of three representative derivatives are presented.

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