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CAS

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426206-77-1

Cyclohexanone, 2-ethenyl-3-(1-methylethyl)-, (2R,3R)-rel- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 426206-77-1 Structure

  • Basic information

    1. Product Name: Cyclohexanone, 2-ethenyl-3-(1-methylethyl)-, (2R,3R)-rel- (9CI)
    2. Synonyms: Cyclohexanone, 2-ethenyl-3-(1-methylethyl)-, (2R,3R)-rel- (9CI)
    3. CAS NO:426206-77-1
    4. Molecular Formula: C11H18O
    5. Molecular Weight: 166.26002
    6. EINECS: N/A
    7. Product Categories: ISOPROPYL
    8. Mol File: 426206-77-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclohexanone, 2-ethenyl-3-(1-methylethyl)-, (2R,3R)-rel- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanone, 2-ethenyl-3-(1-methylethyl)-, (2R,3R)-rel- (9CI)(426206-77-1)
    11. EPA Substance Registry System: Cyclohexanone, 2-ethenyl-3-(1-methylethyl)-, (2R,3R)-rel- (9CI)(426206-77-1)

  • 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: 426206-77-1(Hazardous Substances Data)

426206-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 426206-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,6,2,0 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 426206-77:
(8*4)+(7*2)+(6*6)+(5*2)+(4*0)+(3*6)+(2*7)+(1*7)=131
131 % 10 = 1
So 426206-77-1 is a valid CAS Registry Number.

426206-77-1Downstream Products

426206-77-1Relevant articles and documents

Equatorial preference in the GaCl3-promoted ethenylation of cyclic ketones

Arisawa,Miyagawa,Yamaguchi

, p. 138 - 145 (2007/10/03)

Silyl enol ethers derived from substituted cyclohexanones are ethenylated with trimethylsilylethyne in the presence of GaCl3. Carbon-carbon bond formation was completed in less than 5 min at room temperature and protodegallation of the organogallium intermediate formed with 6 M sulfuric acid gave β-enones. The reactions exhibit a bias for the equatorial C-C bond formation, which contrasts the axial stereochemistry of enolate alkylation. The origin of this stereoselectivity is discussed.

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