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400828-09-3

Cyclohexanecarboxylic acid, 2-oxo-1-(3-phenyl-2-propenyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 400828-09-3 Structure

  • Basic information

    1. Product Name: Cyclohexanecarboxylic acid, 2-oxo-1-(3-phenyl-2-propenyl)-, ethyl ester
    2. Synonyms:
    3. CAS NO:400828-09-3
    4. Molecular Formula: C18H22O3
    5. Molecular Weight: 286.371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 400828-09-3.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: Cyclohexanecarboxylic acid, 2-oxo-1-(3-phenyl-2-propenyl)-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanecarboxylic acid, 2-oxo-1-(3-phenyl-2-propenyl)-, ethyl ester(400828-09-3)
    11. EPA Substance Registry System: Cyclohexanecarboxylic acid, 2-oxo-1-(3-phenyl-2-propenyl)-, ethyl ester(400828-09-3)

  • 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: 400828-09-3(Hazardous Substances Data)

400828-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 400828-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,8,2 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 400828-09:
(8*4)+(7*0)+(6*0)+(5*8)+(4*2)+(3*8)+(2*0)+(1*9)=113
113 % 10 = 3
So 400828-09-3 is a valid CAS Registry Number.

400828-09-3Downstream Products

400828-09-3Relevant articles and documents

Pd-Catalyzed Alkene Difunctionalization Reactions of Malonate Nucleophiles: Synthesis of Substituted Cyclopentanes via Alkene Aryl-Alkylation and Akenyl-Alkylation

White, Derick R.,Hinds, Elsa M.,Bornowski, Evan C.,Wolfe, John P.

, p. 3813 - 3816 (2019)

The Pd-catalyzed coupling of malonate nucleophiles with alkenes bearing tethered aryl or alkenyl triflates is described. These alkene difunctionalization reactions afford malonate-substituted cyclopentanes that contain fused aryl or cycloalkenyl rings. Th

Pd-Catalyzed Alkene Difunctionalization Reactions of Enolates for the Synthesis of Substituted Bicyclic Cyclopentanes

Bornowski, Evan C.,Hinds, Elsa M.,White, Derick R.,Nakamura, Yusuke,Wolfe, John P.

, p. 1610 - 1630 (2019/09/04)

Palladium-catalyzed alkene difunctionalization reactions between alkenes bearing tethered aryl or alkenyl triflates and enolate nucleophiles are described. The transformations form two C-C bonds, a ring, and up to two stereocenters while producing substit

Construction of vicinal tertiary and all-carbon quaternary stereocenters via Ir-catalyzed regio-, diastereo-, and enantioselective allylic alkylation and applications in sequential Pd catalysis

Liu, Wen-Bo,Reeves, Corey M.,Virgil, Scott C.,Stoltz, Brian M.

supporting information, p. 10626 - 10629 (2013/08/23)

Highly congested vicinal stereocenters comprised of tertiary and all-carbon quaternary centers were generated via Ir-catalyzed asymmetric allylic alkylation of β-ketoesters. These catalytic reactions proceed in excellent yields with a broad scope on either reaction partner and with outstanding regio-, diastereo-, and enantiocontrol. Implementation of a subsequent Pd-catalyzed alkylation affords dialkylated products with pinpoint stereochemical control of both chiral centers.

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