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7-Methoxy-1,1,4-tris-(4-methoxy-phenyl)-1,2,3,4-tetrahydro-naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104267-17-6 Structure
  • Basic information

    1. Product Name: 7-Methoxy-1,1,4-tris-(4-methoxy-phenyl)-1,2,3,4-tetrahydro-naphthalene
    2. Synonyms: 7-Methoxy-1,1,4-tris-(4-methoxy-phenyl)-1,2,3,4-tetrahydro-naphthalene
    3. CAS NO:104267-17-6
    4. Molecular Formula:
    5. Molecular Weight: 480.604
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104267-17-6.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: 7-Methoxy-1,1,4-tris-(4-methoxy-phenyl)-1,2,3,4-tetrahydro-naphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Methoxy-1,1,4-tris-(4-methoxy-phenyl)-1,2,3,4-tetrahydro-naphthalene(104267-17-6)
    11. EPA Substance Registry System: 7-Methoxy-1,1,4-tris-(4-methoxy-phenyl)-1,2,3,4-tetrahydro-naphthalene(104267-17-6)
  • 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: 104267-17-6(Hazardous Substances Data)

104267-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104267-17-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,6 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104267-17:
(8*1)+(7*0)+(6*4)+(5*2)+(4*6)+(3*7)+(2*1)+(1*7)=96
96 % 10 = 6
So 104267-17-6 is a valid CAS Registry Number.

104267-17-6Downstream Products

104267-17-6Relevant articles and documents

Surface Photochemistry: The CdS-Mediated Reactions of 1,1-Di-p-anisyletylene

Al-Ekabi, H.,Mayo, P. de

, p. 4756 - 4759 (1987)

The CdS-photomediated reaction of 1,1-di-p-anisylethylene (1b) leads to the formation of two cyclized (2 + 4) and two open chain dimeric products.All for reactions were quenched by 1,2,4,5-tetramethoxybenzene.Comparision of the product distribution in the CdS-induced reaction with those obtained by using cyanoaromatic sensitizers showed that the CdS distribution fell within the range found in the homogeneous systems by varying the nature of the sensitizer and of the solvent.It can be concluded that in this system, at least, the fact of adsorption on the semiconductor surface plays a minor role in directing the nature of the products.One sample of CdS used, which was of high purity, appeared able, even when washed, to induce the acid-catalyzed "dark" dimerization of 1b.This sample yielded, on irradiation, the same four dimeric materials obtained previously, together with 1,2-dimethyltetra-p-anisylethane.

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