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CAS

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138404-01-0

Cyclohexanecarboxylic acid, 2-ethyl-1-hydroxy-6-(4-methoxyphenyl)-3-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138404-01-0 Structure

  • Basic information

    1. Product Name: Cyclohexanecarboxylic acid, 2-ethyl-1-hydroxy-6-(4-methoxyphenyl)-3-oxo-
    2. Synonyms:
    3. CAS NO:138404-01-0
    4. Molecular Formula: C16H20O5
    5. Molecular Weight: 292.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138404-01-0.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: Cyclohexanecarboxylic acid, 2-ethyl-1-hydroxy-6-(4-methoxyphenyl)-3-oxo-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanecarboxylic acid, 2-ethyl-1-hydroxy-6-(4-methoxyphenyl)-3-oxo-(138404-01-0)
    11. EPA Substance Registry System: Cyclohexanecarboxylic acid, 2-ethyl-1-hydroxy-6-(4-methoxyphenyl)-3-oxo-(138404-01-0)

  • 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: 138404-01-0(Hazardous Substances Data)

138404-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138404-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,0 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138404-01:
(8*1)+(7*3)+(6*8)+(5*4)+(4*0)+(3*4)+(2*0)+(1*1)=110
110 % 10 = 0
So 138404-01-0 is a valid CAS Registry Number.

138404-01-0Relevant articles and documents

Structural Parallels Between the Cardiotonic Steroids and the Erythrophleum Alkaloids - I. Synthesis of Phenanthrenone Precursors to Novel Erythrophleum Alkaloid Analogues

Baker, Robert W.,Knox, John R.,Rogers, Dan H.

, p. 7951 - 7964 (1991)

(4aR*, 10R*, 10aR*)-10-Hydroxy-7-methoxy-3,4,4a,9,10,10a-hexahydrophenanthren-2(1H)-one (3) has been synthesised with the key step involving intramolecular electrophilic alkylation of the aromatic ring, via a Pummerer rear

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