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1449490-04-3

C88H66N2O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1449490-04-3 Structure

  • Basic information

    1. Product Name: C88H66N2O4
    2. Synonyms: C88H66N2O4
    3. CAS NO:1449490-04-3
    4. Molecular Formula:
    5. Molecular Weight: 1215.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1449490-04-3.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: C88H66N2O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C88H66N2O4(1449490-04-3)
    11. EPA Substance Registry System: C88H66N2O4(1449490-04-3)

  • 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: 1449490-04-3(Hazardous Substances Data)

1449490-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1449490-04-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,4,9 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1449490-04:
(9*1)+(8*4)+(7*4)+(6*9)+(5*4)+(4*9)+(3*0)+(2*0)+(1*4)=183
183 % 10 = 3
So 1449490-04-3 is a valid CAS Registry Number.

1449490-04-3Upstream product

1449490-04-3Downstream Products

1449490-04-3Relevant articles and documents

Convergent synthesis of hexameric naphthylene macrocycles with dicarboxylic imide appendages

Xue, Jing Yang,Nakanishi, Waka,Tanimoto, Daiki,Hara, Daisuke,Nakamura, Yuta,Isobe, Hiroyuki

, p. 4963 - 4965 (2013)

A series of macrocyclic compounds, [6]cyclo-2,7-naphthylenes ([6]CNAP), composed of six naphthylene units are synthesized through a [3+3] convergent route in good to moderate yields. The synthesis method allowed for the introduction of dicarboxylic imide moieties to the naphthylene units. Crystallographic analysis of a derivative possessing four imide groups showed a trimeric columnar assembly with an alignment of nanometer-sized macrocyclic pores.

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