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CAS

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1016984-17-0

3-(2,4,6-Trimethylphenyl)-1-methyl-1-phenyl-1H-indene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1016984-17-0 Structure

  • Basic information

    1. Product Name: 3-(2,4,6-Trimethylphenyl)-1-methyl-1-phenyl-1H-indene
    2. Synonyms:
    3. CAS NO:1016984-17-0
    4. Molecular Formula:
    5. Molecular Weight: 324.466
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1016984-17-0.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: 3-(2,4,6-Trimethylphenyl)-1-methyl-1-phenyl-1H-indene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2,4,6-Trimethylphenyl)-1-methyl-1-phenyl-1H-indene(1016984-17-0)
    11. EPA Substance Registry System: 3-(2,4,6-Trimethylphenyl)-1-methyl-1-phenyl-1H-indene(1016984-17-0)

  • 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: 1016984-17-0(Hazardous Substances Data)

1016984-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1016984-17-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,6,9,8 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1016984-17:
(9*1)+(8*0)+(7*1)+(6*6)+(5*9)+(4*8)+(3*4)+(2*1)+(1*7)=150
150 % 10 = 0
So 1016984-17-0 is a valid CAS Registry Number.

1016984-17-0Downstream Products

1016984-17-0Relevant articles and documents

Reactions of arylacetylenic compounds with arenes in the presence of aluminum halides

Shchukin,Vasil'Ev,Grinenko

, p. 82 - 97 (2010)

Conjugated arylacetylenic ketones and aldehydes, propargyl-type alcohols, and arylacetylenes reacted with arenes in the presence of AlBr3 or AlCl3 as catalyst to give substituted indenes. 3-Arylpropynoic acids under analogous conditi

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