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CAS

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126784-53-0

(2R*,6R*)-2-ethoxycarbonyl-2,6-dimethylcyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126784-53-0 Structure

  • Basic information

    1. Product Name: (2R*,6R*)-2-ethoxycarbonyl-2,6-dimethylcyclohexanone
    2. Synonyms:
    3. CAS NO:126784-53-0
    4. Molecular Formula:
    5. Molecular Weight: 198.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126784-53-0.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: (2R*,6R*)-2-ethoxycarbonyl-2,6-dimethylcyclohexanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R*,6R*)-2-ethoxycarbonyl-2,6-dimethylcyclohexanone(126784-53-0)
    11. EPA Substance Registry System: (2R*,6R*)-2-ethoxycarbonyl-2,6-dimethylcyclohexanone(126784-53-0)

  • 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: 126784-53-0(Hazardous Substances Data)

126784-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126784-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,8 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126784-53:
(8*1)+(7*2)+(6*6)+(5*7)+(4*8)+(3*4)+(2*5)+(1*3)=150
150 % 10 = 0
So 126784-53-0 is a valid CAS Registry Number.

126784-53-0Relevant articles and documents

Total Synthesis of (±)-Waihoensene

Lee, Hongsoo,Kang, Taek,Lee, Hee-Yoon

, p. 8254 - 8257 (2017)

The first total synthesis of waihoensene, a tetracyclic diterpene containing an angular triquinane and a six-membered ring, with four contiguous quaternary carbon atoms, was achieved through the tandem cycloaddition reaction of an allenyl diazo substrate containing a six-membered ring via trimethylenemethane (TMM) diyl intermediate.

A SYNTHESIS OF (-)-DEOXYPODOCARPIC ACID METHYL ESTER VIA AN ENZYMATIC ENANTIOSELECTIVE HYDROLYSIS OF THE KEY INTERMEDIATE ENOL ESTER

Sugai, Takeshi,Kakeya, Hideaki,Ohta, Hiromichi,Morooka, Mitsuo,Ohba, Shigeru

, p. 6135 - 6144 (2007/10/02)

(1R,4aR,10aS)-(-)-1-Methoxycarbonyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene (deoxypodocarpic acid methyl ester 1), a useful intermediate for the synthesis of various diterpenes, was synthesized from (R)-(+)-6-ethoxycarbonyl-2,6-dimethyl-1-

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