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10383-75-2

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

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  • 10383-75-2 Structure

  • Basic information

    1. Product Name: 14-Phenyldibenzaceanthrylene
    2. Synonyms:
    3. CAS NO:10383-75-2
    4. Molecular Formula:
    5. Molecular Weight: 378.473
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10383-75-2.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: 14-Phenyldibenzaceanthrylene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 14-Phenyldibenzaceanthrylene(10383-75-2)
    11. EPA Substance Registry System: 14-Phenyldibenzaceanthrylene(10383-75-2)

  • 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: 10383-75-2(Hazardous Substances Data)

10383-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10383-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,8 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10383-75:
(7*1)+(6*0)+(5*3)+(4*8)+(3*3)+(2*7)+(1*5)=82
82 % 10 = 2
So 10383-75-2 is a valid CAS Registry Number.

10383-75-2Upstream product

10383-75-2Downstream Products

10383-75-2Relevant articles and documents

Tellurium-Mediated Halogen Transer from Polyhaloalkanes to Diyne Acceptors

Blum, Jochanan,Baidossi, Wael,Badriech, Yacoub,Hoffman, Roy E.,Schumann, Herbert

, p. 4738 - 4742 (1995)

Elemental tellurium catalyzes transfer of halogen from (CHCl2)2, from C2HCl5 and from (CHBr2)2, to the phenylated diynes 1-3, 17, 20, and 24, in which the alkyne moieties are in close proximity.The process is associated with cyclorearrangement reactions by which halogenated polycycles are formed.In boiling C2HCl5, derivatives of 1,2-bis(phenylethynyl)benzenes afford 5-halogenated indenoindenes, 1,8-bis(phenylethynyl)naphthalene gives a chlorinated benzofluoranthene derivative, and 2,2'-bis(phenylethynyl) forms 9-chloro-14-phenylbenzanthracene.Diynes 25 and 26 in which the ethynyl functions are further removed from each other fail to yield halogenated products.Diyne 25 undergoes oxidative cyclization by which 1,3-diphenyldibenzocycloheptafuran (29) is formed.Compound 26 is transformed to hydrocarbon 32, which involves a phenyl ring walk and elimination of H2Te.

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