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860766-80-9

4-[2-(2-methoxyphenyl)ethyl]phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 860766-80-9 Structure

  • Basic information

    1. Product Name: 4-[2-(2-methoxyphenyl)ethyl]phenol
    2. Synonyms: 4-[2-(2-methoxyphenyl)ethyl]phenol
    3. CAS NO:860766-80-9
    4. Molecular Formula:
    5. Molecular Weight: 228.291
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 860766-80-9.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: 4-[2-(2-methoxyphenyl)ethyl]phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[2-(2-methoxyphenyl)ethyl]phenol(860766-80-9)
    11. EPA Substance Registry System: 4-[2-(2-methoxyphenyl)ethyl]phenol(860766-80-9)

  • 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: 860766-80-9(Hazardous Substances Data)

860766-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 860766-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,7,6 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 860766-80:
(8*8)+(7*6)+(6*0)+(5*7)+(4*6)+(3*6)+(2*8)+(1*0)=199
199 % 10 = 9
So 860766-80-9 is a valid CAS Registry Number.

860766-80-9Relevant articles and documents

Easy eco-friendly phenonium ion production from phenethyl alcohols in dimethyl carbonate

Barontini,Proietti Silvestri,Nardi,Bovicelli,Pari,Gallucci,Spezia,Righi

supporting information, p. 5004 - 5006 (2013/08/28)

An efficient and simple one-pot procedure for selective etherification of 2-aryl-ethylalcohols has been achieved through Amberlyst 15-catalyzed reaction in dimethyl carbonate (DMC). Moreover, the polymer catalyst could be recovered and reused with no effect on its activity. The reaction mechanism involves the formation of phenonium ion which has been demonstrated by a C-C bond forming reaction. Theoretical studies are in agreement with and thus explain experimental results.

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