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140709-73-5

Cyclohexanecarboxylic acid, 1-(4-methoxy-4-oxo-2-butenyl)-2-methylene-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 140709-73-5 Structure

  • Basic information

    1. Product Name: Cyclohexanecarboxylic acid, 1-(4-methoxy-4-oxo-2-butenyl)-2-methylene-, ethyl ester
    2. Synonyms:
    3. CAS NO:140709-73-5
    4. Molecular Formula: C15H22O4
    5. Molecular Weight: 266.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 140709-73-5.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: Cyclohexanecarboxylic acid, 1-(4-methoxy-4-oxo-2-butenyl)-2-methylene-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanecarboxylic acid, 1-(4-methoxy-4-oxo-2-butenyl)-2-methylene-, ethyl ester(140709-73-5)
    11. EPA Substance Registry System: Cyclohexanecarboxylic acid, 1-(4-methoxy-4-oxo-2-butenyl)-2-methylene-, ethyl ester(140709-73-5)

  • 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: 140709-73-5(Hazardous Substances Data)

140709-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140709-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,7,0 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 140709-73:
(8*1)+(7*4)+(6*0)+(5*7)+(4*0)+(3*9)+(2*7)+(1*3)=115
115 % 10 = 5
So 140709-73-5 is a valid CAS Registry Number.

140709-73-5Downstream Products

140709-73-5Relevant articles and documents

Control of Ring-Junction Stereochemistry via Radical Cyclization. A New Construction of trans-Decalins

Kawaguchi, Mami,Satoh, Shoji,Mori, Miwako,Shibasaki, Masakatsu

, p. 395 - 398 (2007/10/02)

A stereoselective synthesis of trans-decalins has been developed by use of regiocontrolled 6-endo-trig-radical cyclization of alkenyl bromides with an exo-methylene group in cyclohexane ring.

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