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1-Cyclohex-2-enyl-5-methylhexan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 158233-84-2 Structure
  • Basic information

    1. Product Name: 1-Cyclohex-2-enyl-5-methylhexan-2-one
    2. Synonyms:
    3. CAS NO:158233-84-2
    4. Molecular Formula:
    5. Molecular Weight: 194.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 158233-84-2.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: 1-Cyclohex-2-enyl-5-methylhexan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Cyclohex-2-enyl-5-methylhexan-2-one(158233-84-2)
    11. EPA Substance Registry System: 1-Cyclohex-2-enyl-5-methylhexan-2-one(158233-84-2)
  • 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: 158233-84-2(Hazardous Substances Data)

158233-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158233-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,2,3 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 158233-84:
(8*1)+(7*5)+(6*8)+(5*2)+(4*3)+(3*3)+(2*8)+(1*4)=142
142 % 10 = 2
So 158233-84-2 is a valid CAS Registry Number.

158233-84-2Downstream Products

158233-84-2Relevant articles and documents

Ketone-directed peracid epoxidation of cyclic alkenes

Armstrong, Alan,Barsanti, Paul A.,Clarke, Paul A.,Wood, Anthony

, p. 1373 - 1380 (1996)

Ketone carbonyl groups are shown to direct the peracid epoxidation of cyclic alkenes with greater selectivity than that displayed by esters. An 18O labelling study is used to show that a dioxirane intermediate is not involved in these reactions.

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