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29304-62-9

6-methyl-4-phenyl-1,2-dihydro-naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29304-62-9 Structure

  • Basic information

    1. Product Name: 6-methyl-4-phenyl-1,2-dihydro-naphthalene
    2. Synonyms: 6-methyl-4-phenyl-1,2-dihydro-naphthalene
    3. CAS NO:29304-62-9
    4. Molecular Formula:
    5. Molecular Weight: 220.314
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29304-62-9.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: 6-methyl-4-phenyl-1,2-dihydro-naphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-methyl-4-phenyl-1,2-dihydro-naphthalene(29304-62-9)
    11. EPA Substance Registry System: 6-methyl-4-phenyl-1,2-dihydro-naphthalene(29304-62-9)

  • 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: 29304-62-9(Hazardous Substances Data)

29304-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29304-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,0 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29304-62:
(7*2)+(6*9)+(5*3)+(4*0)+(3*4)+(2*6)+(1*2)=109
109 % 10 = 9
So 29304-62-9 is a valid CAS Registry Number.

29304-62-9Downstream Products

29304-62-9Relevant articles and documents

FeCl3-catalyzed intramolecular hydroarylation of alkynes

Dal Zotto, Christophe,Wehbe, Johny,Virieux, David,Campagne, Jean-Marc

scheme or table, p. 2033 - 2035 (2009/04/07)

The intramolecular hydroarylation of alkynes using a substoichiometric amount of FeCl3 is described. When starting from tetrasubstituted substrates, products resulting from an unexpected toluene (or xylene) elimination are isolated in good yields.

Thermolysis of Phenyl-substituted 1,2-Dihydronaphthalenes. Evidence for Diphenylbutadienes as Intermediates

Lamberts, Joseph J. M.,Cuppen, Theo J. H. M.,Laarhoven, Wim H.

, p. 1819 - 1828 (2007/10/02)

The thermal rearrangement of the four phenyl-substituted 1,2-dihydronaphthalenes (15), (16), (19), and (20) have been studied by flash vacuum pyrolysis (FVP).By using the deuteriated starting compounds -(15) and -(16), it has been established that 1- and 4-phenyl-1,2-dihydronaphthalene (15) and (19) and 2- and 3-phenyl-1,2-dihydronaphthalene (16) and (20) are interconverted via the intermediates 1- and 2-phenyl-2,3-dihydronaphthalene (17) and (18), respectively, through two consecutive, sigmatropic 1,5-hydrogen shifts.In both processes partial oxidation to the corresponding phenylnaphthalenes (21) and (22) takes place.The deuterium distribution in the pyrolysis products suggests that in the hot zone diphenylbutadienes are formed, which are reconverted into phenyldihydronaphthalenes upon reaching the cold receiving flask.By FVP of 4-(p-tolyl)-1,2-dihydronaphthalene (34), 1-phenyl-1-(p-tolyl)butadiene (39), and 1-phenyl-4-(p-tolyl)butadiene (45) the latter type of interconversion could be confirmed.

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