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CAS

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1122620-33-0

3-(2-methylbut-1-enyl)-6-methylcyclohexa-1,5-dienyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1122620-33-0 Structure

  • Basic information

    1. Product Name: 3-(2-methylbut-1-enyl)-6-methylcyclohexa-1,5-dienyl acetate
    2. Synonyms: 3-(2-methylbut-1-enyl)-6-methylcyclohexa-1,5-dienyl acetate
    3. CAS NO:1122620-33-0
    4. Molecular Formula:
    5. Molecular Weight: 206.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1122620-33-0.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: 3-(2-methylbut-1-enyl)-6-methylcyclohexa-1,5-dienyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-methylbut-1-enyl)-6-methylcyclohexa-1,5-dienyl acetate(1122620-33-0)
    11. EPA Substance Registry System: 3-(2-methylbut-1-enyl)-6-methylcyclohexa-1,5-dienyl acetate(1122620-33-0)

  • 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: 1122620-33-0(Hazardous Substances Data)

1122620-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1122620-33-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,2,6,2 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1122620-33:
(9*1)+(8*1)+(7*2)+(6*2)+(5*6)+(4*2)+(3*0)+(2*3)+(1*3)=90
90 % 10 = 0
So 1122620-33-0 is a valid CAS Registry Number.

1122620-33-0Upstream product

1122620-33-0Relevant articles and documents

Gold-catalyzed cycloisomerization of cyclopropyl alkynyl acetates: A versatile approach to 5-, 6-, and 7-membered carbocycles

Zou, Yue,Garayalde, David,Wang, Quanrui,Nevado, Cristina,Goeke, Andreas,Ito, Yoshihiko

, p. 10110 - 10113 (2008)

Nonclassical chirality transfer? Depending on the substitution pattern of propargyl acetates, a gold-catalyzed homologous Rautenstrauch reaction generates either 5- or 6-membered ring systems (see scheme). The stabilization of cationic intermediates is crucial for this reaction to succeed. The underlying principle for the good chirality transfer observed could be gold-stabilized nonclassical carbocations having configurational stability.

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