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300807-61-8

C58H59NO14Se is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 300807-61-8 Structure

  • Basic information

    1. Product Name: C58H59NO14Se
    2. Synonyms: C58H59NO14Se
    3. CAS NO:300807-61-8
    4. Molecular Formula:
    5. Molecular Weight: 1073.06
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 300807-61-8.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: C58H59NO14Se(CAS DataBase Reference)
    10. NIST Chemistry Reference: C58H59NO14Se(300807-61-8)
    11. EPA Substance Registry System: C58H59NO14Se(300807-61-8)

  • 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: 300807-61-8(Hazardous Substances Data)

300807-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 300807-61-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,0,8,0 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 300807-61:
(8*3)+(7*0)+(6*0)+(5*8)+(4*0)+(3*7)+(2*6)+(1*1)=98
98 % 10 = 8
So 300807-61-8 is a valid CAS Registry Number.

300807-61-8Downstream Products

300807-61-8Relevant articles and documents

Synthesis, characterization, and controlling morphology of an aryl ether dendrimer containing a dichalcogenide bond as the core

Takaguchi,Suzuki,Mori,Motoyoshiya,Aoyama

, p. 1857 - 1860 (2000)

A poly(benzyl ether) dendron with a thiol group or a selenocyanate group at the focal point was synthesized and well characterized, and then used for the controlling morphology. The molecules show a reversible redox behavior between dendrons and dendrimer dichalcogenides, being achieved under chemical reactions, although a dendrimer having selenium atoms has never been reported. Furthermore, dendrimer dichalcogenides underwent an dechalcogenation reaction upon a treatment with hexaethylphosphorous triamide or photoirradiation to give dendrimer chalcogenides.

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