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CAS

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1446518-52-0

2-acetyl-2-(3-phenoxyprop-1-en-2-yl)cyclopentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446518-52-0 Structure

  • Basic information

    1. Product Name: 2-acetyl-2-(3-phenoxyprop-1-en-2-yl)cyclopentanone
    2. Synonyms: 2-acetyl-2-(3-phenoxyprop-1-en-2-yl)cyclopentanone
    3. CAS NO:1446518-52-0
    4. Molecular Formula:
    5. Molecular Weight: 258.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446518-52-0.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: 2-acetyl-2-(3-phenoxyprop-1-en-2-yl)cyclopentanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-acetyl-2-(3-phenoxyprop-1-en-2-yl)cyclopentanone(1446518-52-0)
    11. EPA Substance Registry System: 2-acetyl-2-(3-phenoxyprop-1-en-2-yl)cyclopentanone(1446518-52-0)

  • 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: 1446518-52-0(Hazardous Substances Data)

1446518-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446518-52-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,5,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1446518-52:
(9*1)+(8*4)+(7*4)+(6*6)+(5*5)+(4*1)+(3*8)+(2*5)+(1*2)=170
170 % 10 = 0
So 1446518-52-0 is a valid CAS Registry Number.

1446518-52-0Downstream Products

1446518-52-0Relevant articles and documents

Palladium-Catalysed Construction of All-Carbon Quaternary Centres with Propargylic Electrophiles: Challenges in the Simultaneous Control of Regio-, Chemo- and Enantioselectivity

Kenny, Miles,Schr?der, Sybrin P.,Taylor, Nicholas J.,Jackson, Paula,Kitson, Daniel J.,Franckevi?ius, Vilius

, p. 1796 - 1814 (2018)

This article describes the palladium-catalysed three-component coupling of 1,3-dicarbonyl compounds with nucleophiles and propargylic electrophiles for the generation of quaternary all-carbon centres in a single step, which necessitates the simultaneous control of regio-, chemo- and enantioselectivity. The use of propargyl enol carbonates, the source of two of the components, was found to be essential in maintaining high levels of regiocontrol and chemoselectivity, whereas a careful analysis of p K a trends of O-, C- and N-nucleophiles as the other coupling partner indicates that the highest levels of selectivity are likely to be obtained with relatively acidic species, such as phenols, 1,3-dicarbonyl compounds and aromatic N-heterocycles. Finally, studies towards the development of the catalytic enantioselective construction of quaternary all-carbon centres by means of alkenylation and allylic alkylation are disclosed.

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