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114469-02-2

2-(dimethoxymethyl)-α-phenyl-1-naphthalenemethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114469-02-2 Structure

  • Basic information

    1. Product Name: 2-(dimethoxymethyl)-α-phenyl-1-naphthalenemethanol
    2. Synonyms: 2-(dimethoxymethyl)-α-phenyl-1-naphthalenemethanol
    3. CAS NO:114469-02-2
    4. Molecular Formula:
    5. Molecular Weight: 308.377
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114469-02-2.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: 2-(dimethoxymethyl)-α-phenyl-1-naphthalenemethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(dimethoxymethyl)-α-phenyl-1-naphthalenemethanol(114469-02-2)
    11. EPA Substance Registry System: 2-(dimethoxymethyl)-α-phenyl-1-naphthalenemethanol(114469-02-2)

  • 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: 114469-02-2(Hazardous Substances Data)

114469-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114469-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,6 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114469-02:
(8*1)+(7*1)+(6*4)+(5*4)+(4*6)+(3*9)+(2*0)+(1*2)=112
112 % 10 = 2
So 114469-02-2 is a valid CAS Registry Number.

114469-02-2Relevant articles and documents

1-Phenylisobenzofuran, 1-Phenylnaphthofuran, 1-Phenylnaphthofuran, and 3-Phenylnaphthofuran via Cyclic Hemiaminal, Hemiacetal, and Acetal Precursors

Smith, James G.,Fogg, Deryn E.,Munday, Ian J.,Sandborn, Richard E.,Dibble, Peter W.

, p. 2942 - 2953 (2007/10/02)

The title compounds have been generated via cyclic hemiaminal, hemiacetal, and acetal precursors and trapped in Diels-Alder reactions with several dienophiles.The precursors are easily prepared from o-bromobenzyl alcohol, 2-bromo-3-naphthalenemethanol, or

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