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1408003-35-9

(E)-2-(3-acetoxy-2-cyclohexyl)-1-phenylethan-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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  • 1408003-35-9 Structure

  • Basic information

    1. Product Name: (E)-2-(3-acetoxy-2-cyclohexyl)-1-phenylethan-1-one
    2. Synonyms: (E)-2-(3-acetoxy-2-cyclohexyl)-1-phenylethan-1-one
    3. CAS NO:1408003-35-9
    4. Molecular Formula:
    5. Molecular Weight: 258.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1408003-35-9.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: (E)-2-(3-acetoxy-2-cyclohexyl)-1-phenylethan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-2-(3-acetoxy-2-cyclohexyl)-1-phenylethan-1-one(1408003-35-9)
    11. EPA Substance Registry System: (E)-2-(3-acetoxy-2-cyclohexyl)-1-phenylethan-1-one(1408003-35-9)

  • 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: 1408003-35-9(Hazardous Substances Data)

1408003-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1408003-35-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,8,0,0 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1408003-35:
(9*1)+(8*4)+(7*0)+(6*8)+(5*0)+(4*0)+(3*3)+(2*3)+(1*5)=109
109 % 10 = 9
So 1408003-35-9 is a valid CAS Registry Number.

1408003-35-9Downstream Products

1408003-35-9Relevant articles and documents

InCl3/Me3SiCl-catalyzed direct michael addition of enol acetates to α,β-unsaturated ketones

Onishi, Yoshiharu,Yoneda, Yuki,Nishimoto, Yoshihiro,Yasuda, Makoto,Baba, Akio

, p. 5788 - 5791 (2012)

The direct Michael addition of enol acetates to α,β-unsaturated ketones was achieved using a combination of Lewis acid catalysts, InCl 3 and Me3SiCl, which furnished stable enol-form products that could be further transformed into functionalized 1,5-diketones by reactions with various electrophiles.

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