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1-(cyclohex-2-enyl)-3-phenylpropan-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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  • 221253-04-9 Structure
  • Basic information

    1. Product Name: 1-(cyclohex-2-enyl)-3-phenylpropan-2-one
    2. Synonyms: 1-(cyclohex-2-enyl)-3-phenylpropan-2-one
    3. CAS NO:221253-04-9
    4. Molecular Formula:
    5. Molecular Weight: 214.307
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 221253-04-9.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)-3-phenylpropan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(cyclohex-2-enyl)-3-phenylpropan-2-one(221253-04-9)
    11. EPA Substance Registry System: 1-(cyclohex-2-enyl)-3-phenylpropan-2-one(221253-04-9)
  • 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: 221253-04-9(Hazardous Substances Data)

221253-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221253-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,2,5 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 221253-04:
(8*2)+(7*2)+(6*1)+(5*2)+(4*5)+(3*3)+(2*0)+(1*4)=79
79 % 10 = 9
So 221253-04-9 is a valid CAS Registry Number.

221253-04-9Relevant articles and documents

Asymmetric allylic alkylation of ketone enolates: An asymmetric claisen surrogate

Burger, Erin C.,Tunge, Jon A.

, p. 4113 - 4115 (2007/10/03)

(Chemical Equation Presented) The combination of catalytic palladium(0) and Trost ligand provides an effective catalyst for the rearrangement of allyl β-ketoesters. The mechanism of the transformation involves formation of π-allyl palladium intermediates which undergo enantioselective attack by ketone enolates. Decarboxylation of β-ketocarboxylates allows regiospecific generation of enolates under extremely mild conditions.

Ring opening of cyclopropane in tricyclo[4.3.0.02,9]nonan-3-one with electrophile-nucleophile reagents

Fernandez-Mateos, A.,Alonso, J. J. Perez,Gonzales, R. Rubio

, p. 847 - 860 (2007/10/03)

Four tricyclo[4.3.0.02,9]nonan-3-one systems were treated with TBDMSI, TMSTFA and TMSTFA/NaSPh, affording different cyclopropane cleavage products, depending on the location of the substituent and the nature of the reagent.

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