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879894-13-0

Cycloheptanol, 1-(2,3-dimethoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 879894-13-0 Structure

  • Basic information

    1. Product Name: Cycloheptanol, 1-(2,3-dimethoxyphenyl)-
    2. Synonyms:
    3. CAS NO:879894-13-0
    4. Molecular Formula: C15H22O3
    5. Molecular Weight: 250.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 879894-13-0.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: Cycloheptanol, 1-(2,3-dimethoxyphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cycloheptanol, 1-(2,3-dimethoxyphenyl)-(879894-13-0)
    11. EPA Substance Registry System: Cycloheptanol, 1-(2,3-dimethoxyphenyl)-(879894-13-0)

  • 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: 879894-13-0(Hazardous Substances Data)

879894-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879894-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,8,9 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 879894-13:
(8*8)+(7*7)+(6*9)+(5*8)+(4*9)+(3*4)+(2*1)+(1*3)=260
260 % 10 = 0
So 879894-13-0 is a valid CAS Registry Number.

879894-13-0Relevant articles and documents

Economical and convenient carbonyl transposition approach toward a 2-arylcycloheptanone derivative

Bracca, Andrea B. J.,Kaufman, Teodoro S.

, p. 299 - 310 (2006)

A convenient, straightforward, and easy access to 2(2,3-dimethoxy-phenyl)- cycloheptanone, which employs an heteroatom-facilitated ortho-lithiation coupled to a carbonyl transposition strategy, is reported. The synthetic approach avoids using very expensi

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