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1030607-06-7

C35H36N2O6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1030607-06-7 Structure

  • Basic information

    1. Product Name: C35H36N2O6
    2. Synonyms: C35H36N2O6
    3. CAS NO:1030607-06-7
    4. Molecular Formula:
    5. Molecular Weight: 580.681
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1030607-06-7.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: C35H36N2O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C35H36N2O6(1030607-06-7)
    11. EPA Substance Registry System: C35H36N2O6(1030607-06-7)

  • 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: 1030607-06-7(Hazardous Substances Data)

1030607-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1030607-06-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,6,0 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1030607-06:
(9*1)+(8*0)+(7*3)+(6*0)+(5*6)+(4*0)+(3*7)+(2*0)+(1*6)=87
87 % 10 = 7
So 1030607-06-7 is a valid CAS Registry Number.

1030607-06-7Downstream Products

1030607-06-7Relevant articles and documents

A double ring-closing olefin metathesis approach to [3]catenanes

Gupta, Manav,Kang, Songsu,Mayer, Michael F.

, p. 2946 - 2950 (2008)

A [3]catenane with peripheral olefinic macrocycles was conveniently synthesized via a double ring-closing olefin metathesis. Highlights of this work include the synthesis of a 65-membered macrocycle featuring two phenanthroline ligands, a Cu(I)-templated synthesis of a [3]pseudorotaxane, and the key double ring-closing olefin metathesis to afford the desired [3]catenane in 71% yield.

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