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CAS

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133030-14-5

3-(1,4-Dioxa-spiro[4.5]dec-6-en-6-yl)-cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133030-14-5 Structure

  • Basic information

    1. Product Name: 3-(1,4-Dioxa-spiro[4.5]dec-6-en-6-yl)-cyclohexanone
    2. Synonyms:
    3. CAS NO:133030-14-5
    4. Molecular Formula:
    5. Molecular Weight: 236.311
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133030-14-5.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: 3-(1,4-Dioxa-spiro[4.5]dec-6-en-6-yl)-cyclohexanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(1,4-Dioxa-spiro[4.5]dec-6-en-6-yl)-cyclohexanone(133030-14-5)
    11. EPA Substance Registry System: 3-(1,4-Dioxa-spiro[4.5]dec-6-en-6-yl)-cyclohexanone(133030-14-5)

  • 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: 133030-14-5(Hazardous Substances Data)

133030-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133030-14-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,3 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 133030-14:
(8*1)+(7*3)+(6*3)+(5*0)+(4*3)+(3*0)+(2*1)+(1*4)=65
65 % 10 = 5
So 133030-14-5 is a valid CAS Registry Number.

133030-14-5Downstream Products

133030-14-5Relevant articles and documents

Synthetic applications of Gilman reagents derived from 2-bromo-2-cycloalken-1-one ethylene ketals

Majetich,Leigh,Condon

, p. 605 - 608 (1991)

Gilman reagents derived from 2-bromo-2-cycloalken-1-one ethylene ketals react with allylic, propargylic or benzylic halides to produce functionalized 1,4-dienes while reaction with Michael acceptors gives 1,4-adducts.

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