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38135-10-3

Naphthacene, 5,11-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38135-10-3 Structure

  • Basic information

    1. Product Name: Naphthacene, 5,11-diphenyl-
    2. Synonyms:
    3. CAS NO:38135-10-3
    4. Molecular Formula: C30H20
    5. Molecular Weight: 380.489
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38135-10-3.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: Naphthacene, 5,11-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Naphthacene, 5,11-diphenyl-(38135-10-3)
    11. EPA Substance Registry System: Naphthacene, 5,11-diphenyl-(38135-10-3)

  • 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: 38135-10-3(Hazardous Substances Data)

38135-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38135-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,3 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38135-10:
(7*3)+(6*8)+(5*1)+(4*3)+(3*5)+(2*1)+(1*0)=103
103 % 10 = 3
So 38135-10-3 is a valid CAS Registry Number.

38135-10-3Relevant articles and documents

Electron-Deficient Tetrabenzo-Fused Pyracylene and Conversions into Curved and Planar π-Systems Having Distinct Emission Behaviors

Chaolumen,Murata, Michihisa,Sugano, Yasunori,Wakamiya, Atsushi,Murata, Yasujiro

, p. 9308 - 9312 (2015)

Polycyclic aromatic compounds containing fully unsaturated five-membered ring(s) have been intensively studied because of their unique properties, which include high electron affinity and reactivity. Reported herein is an efficient route for the synthesis

Aryl-perfluoroaryl substituted tetracene: Induction of face-to-face π-π Stacking and enhancement of charge carrier properties

Okamoto, Toshihiro,Nakahara, Katsumasa,Saeki, Akinori,Seki, Shu,Oh, Joon Hak,Akkerman, Hylke B.,Bao, Zhenan,Matsuo, Yutaka

scheme or table, p. 1646 - 1649 (2012/05/05)

5-Perfluorophenyl-11-phenyltetracene (FPPT) having both aryl (Ar) and perfluoroaryl (FAr) groups has been designed and synthesized to obtain well-defined n-n stacking structure of the tetracene core. Single-crystal X-ray analyses as well as photoconductiv

Cross-coupling of 5,11-dibromotetracene catalyzed by a triethylammonium ion tagged diphenylphosphine palladium complex in ionic liquids

Papagni, Antonio,Trombini, Claudio,Lombardo, Marco,Bergantin, Stefano,Chams, Amani,Chiarucci, Michel,Miozzo, Luciano,Parravicini, Matteo

experimental part, p. 4325 - 4329 (2011/10/03)

Suzuki-Miyaura cross-coupling reactions of 5,11-dibromotetracene with arylboronic acids, using a triethylammonium-tagged palladium(II) diphenylphosphine complex as catalyst in a pyrrolidinium-based ionic liquid (IL), allowed the preparation of new 5,11-di

Isomerisations et cyclisations de derives bifonctionnels des diphenyl-1,4 butadienes Z,Z et E,E. Acces a une cetone derivee du Benzo(c) 7H-fluorene

Wehbe, Mohamed,Lepage, Lucette,Lepage, Yves,Platzer, Nicole

, p. 309 - 317 (2007/10/02)

Furannic diols 1a, 1b, furofurans 2a, 2b and stereoisomers (Z,Z) 4 and (E,E) 5a of 2,3 bis phenyl methylene-1,4 diphenyl butanedione give, with strong acids, the -7H benzo(c) fluorenic ketone, 3.The structure of the compound 3 is demonstrated by bidimensi

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