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CAS

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1281318-51-1

2-cyclohexyl-1-(2-methoxyphenyl)ethan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1281318-51-1 Structure

  • Basic information

    1. Product Name: 2-cyclohexyl-1-(2-methoxyphenyl)ethan-1-one
    2. Synonyms: 2-cyclohexyl-1-(2-methoxyphenyl)ethan-1-one
    3. CAS NO:1281318-51-1
    4. Molecular Formula:
    5. Molecular Weight: 232.323
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1281318-51-1.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-cyclohexyl-1-(2-methoxyphenyl)ethan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-cyclohexyl-1-(2-methoxyphenyl)ethan-1-one(1281318-51-1)
    11. EPA Substance Registry System: 2-cyclohexyl-1-(2-methoxyphenyl)ethan-1-one(1281318-51-1)

  • 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: 1281318-51-1(Hazardous Substances Data)

1281318-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1281318-51-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,1,3,1 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1281318-51:
(9*1)+(8*2)+(7*8)+(6*1)+(5*3)+(4*1)+(3*8)+(2*5)+(1*1)=141
141 % 10 = 1
So 1281318-51-1 is a valid CAS Registry Number.

1281318-51-1Relevant articles and documents

An efficient process for the large-scale synthesis of a 2,3,6-trisubstituted indole

Alorati, Anthony D.,Gibb, Andrew D.,Mullens, Peter R.,Stewart, Gavin W.

, p. 1947 - 1952 (2013/03/14)

The efficient synthesis of a key trisubstituted indole intermediate 1 is described. The synthetic route required the use of an aryl Grignard reagent which was not commercially available, and the large-scale formation of this fragment and the thermal evalu

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