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CAS

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1567442-52-7

C18H16O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1567442-52-7 Structure

  • Basic information

    1. Product Name: C18H16O
    2. Synonyms:
    3. CAS NO:1567442-52-7
    4. Molecular Formula:
    5. Molecular Weight: 248.324
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1567442-52-7.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: C18H16O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H16O(1567442-52-7)
    11. EPA Substance Registry System: C18H16O(1567442-52-7)

  • 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: 1567442-52-7(Hazardous Substances Data)

1567442-52-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1567442-52-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,7,4,4 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1567442-52:
(9*1)+(8*5)+(7*6)+(6*7)+(5*4)+(4*4)+(3*2)+(2*5)+(1*2)=187
187 % 10 = 7
So 1567442-52-7 is a valid CAS Registry Number.

1567442-52-7Downstream Products

1567442-52-7Relevant articles and documents

The role of acetylides in dual gold catalysis: A mechanistic investigation of the selectivity difference in the naphthalene synthesis from diynes

Graf, Katharina,Hindenberg, Philip D.,Tokimizu, Yusuke,Naoe, Saori,Rudolph, Matthias,Rominger, Frank,Ohno, Hiroaki,Hashmi, A. Stephen K.

, p. 199 - 204 (2014)

Under the conditions of dual activation catalysis with oxygen nucleophiles, β-substituted naphthalenes were obtained from 1,2-diethinyl arenes. Mechanistic studies, which include isotope labeling experiments, support that dual activation leads to β-substi

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