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2,6-dibenzylnaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113750-28-0 Structure
  • Basic information

    1. Product Name: 2,6-dibenzylnaphthalene
    2. Synonyms:
    3. CAS NO:113750-28-0
    4. Molecular Formula:
    5. Molecular Weight: 308.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113750-28-0.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: 2,6-dibenzylnaphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-dibenzylnaphthalene(113750-28-0)
    11. EPA Substance Registry System: 2,6-dibenzylnaphthalene(113750-28-0)
  • 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: 113750-28-0(Hazardous Substances Data)

113750-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113750-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,5 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 113750-28:
(8*1)+(7*1)+(6*3)+(5*7)+(4*5)+(3*0)+(2*2)+(1*8)=100
100 % 10 = 0
So 113750-28-0 is a valid CAS Registry Number.

113750-28-0Downstream Products

113750-28-0Relevant articles and documents

Direct cross-coupling of benzyl alcohols to construct diarylmethanes via palladium catalysis

Cao, Zhi-Chao,Yu, Da-Gang,Zhu, Ru-Yi,Wei, Jiang-Bo,Shi, Zhang-Jie

, p. 2683 - 2686 (2015)

A direct arylation to furnish diarylmethanes from benzyl alcohols was realized through Pd(PPh3)4-catalyzed Suzuki-Miyaura coupling via benzylic C-O activation in the absence of any additives. The arylation is compatible with various functional groups. This development provides an atom- and step-economic way to approach a diarylmethane scaffold under mild and environmentally benign conditions. This journal is

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