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3-(di-4-anisylphenylmethyl)-6-(di-4-anisylmethylene)-1,4-cyclohexadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102343-05-5 Structure
  • Basic information

    1. Product Name: 3-(di-4-anisylphenylmethyl)-6-(di-4-anisylmethylene)-1,4-cyclohexadiene
    2. Synonyms: 3-(di-4-anisylphenylmethyl)-6-(di-4-anisylmethylene)-1,4-cyclohexadiene
    3. CAS NO:102343-05-5
    4. Molecular Formula:
    5. Molecular Weight: 606.761
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102343-05-5.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: 3-(di-4-anisylphenylmethyl)-6-(di-4-anisylmethylene)-1,4-cyclohexadiene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(di-4-anisylphenylmethyl)-6-(di-4-anisylmethylene)-1,4-cyclohexadiene(102343-05-5)
    11. EPA Substance Registry System: 3-(di-4-anisylphenylmethyl)-6-(di-4-anisylmethylene)-1,4-cyclohexadiene(102343-05-5)
  • 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: 102343-05-5(Hazardous Substances Data)

102343-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102343-05-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,4 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102343-05:
(8*1)+(7*0)+(6*2)+(5*3)+(4*4)+(3*3)+(2*0)+(1*5)=65
65 % 10 = 5
So 102343-05-5 is a valid CAS Registry Number.

102343-05-5Downstream Products

102343-05-5Relevant articles and documents

Protection of nucleosides

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Page 25-27, (2010/02/08)

A process of manufacturing protected nucleosides comprises reacting a nucleoside with a protecting reagent in the presence of a regioselective activator to produce a regioselectively protected nucleoside. In some embodiments of the inventive method, an op

Sterically Hindered Free Radicals. 18. Stabilization of Free Radicals by Substituents As Studied by Using Triphenylmethyls

Neumann, Wilhelm P.,Penenory, Alicia,Stewen, Ulrich,Lehnig, Manfred

, p. 5845 - 5851 (2007/10/02)

The relative stabilization of 10 4-mono- and 24 4,4'-disubstituted triphenylmethyl radicals 1 has been measured by recording the degree of dissociation of the corresponding quinonoid dimers 2 by means of ESR.The following substituents or combinations of t

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