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1616754-77-8

C28H22 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1616754-77-8 Structure

  • Basic information

    1. Product Name: C28H22
    2. Synonyms: C28H22
    3. CAS NO:1616754-77-8
    4. Molecular Formula:
    5. Molecular Weight: 358.483
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1616754-77-8.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: C28H22(CAS DataBase Reference)
    10. NIST Chemistry Reference: C28H22(1616754-77-8)
    11. EPA Substance Registry System: C28H22(1616754-77-8)

  • 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: 1616754-77-8(Hazardous Substances Data)

1616754-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1616754-77-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,6,7,5 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1616754-77:
(9*1)+(8*6)+(7*1)+(6*6)+(5*7)+(4*5)+(3*4)+(2*7)+(1*7)=188
188 % 10 = 8
So 1616754-77-8 is a valid CAS Registry Number.

1616754-77-8Downstream Products

1616754-77-8Relevant articles and documents

Synthesis of Polycyclic Aromatic Hydrocarbons Decorated by Fluorinated Carbon Acids/Carbanions

Hoshikawa, Shoki,Yanai, Hikaru,Martín-Mejías, Irene,Lázaro-Milla, Carlos,Aragoncillo, Cristina,Almendros, Pedro,Matsumoto, Takashi

supporting information, p. 16112 - 16116 (2021/10/12)

The carboarylation reaction of biphenyl-alkynes was successfully triggered by electrophilic attack of 1,1-bis(triflyl)ethylene on the alkyne moiety to give polycyclic aromatic hydrocarbons (PAHs) decorated by superacidic carbon acid functionality. Neutralisation of thus obtained acids with NaHCO3 yielded the corresponding sodium salts, which showed improved solubility in both aqueous and organic solvents.

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