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872369-67-0

(Z)-ethyl 5-phenylpent-3-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 872369-67-0 Structure

  • Basic information

    1. Product Name: (Z)-ethyl 5-phenylpent-3-enoate
    2. Synonyms: (Z)-ethyl 5-phenylpent-3-enoate
    3. CAS NO:872369-67-0
    4. Molecular Formula:
    5. Molecular Weight: 204.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 872369-67-0.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: (Z)-ethyl 5-phenylpent-3-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-ethyl 5-phenylpent-3-enoate(872369-67-0)
    11. EPA Substance Registry System: (Z)-ethyl 5-phenylpent-3-enoate(872369-67-0)

  • 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: 872369-67-0(Hazardous Substances Data)

872369-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872369-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,3,6 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 872369-67:
(8*8)+(7*7)+(6*2)+(5*3)+(4*6)+(3*9)+(2*6)+(1*7)=210
210 % 10 = 0
So 872369-67-0 is a valid CAS Registry Number.

872369-67-0Downstream Products

872369-67-0Relevant articles and documents

Direct oxidative allylic and vinylic amination of alkenes through selenium catalysis

Trenner, Johanna,Depken, Christian,Weber, Thomas,Breder, Alexander

, p. 8952 - 8956 (2013)

Bringing "N" into the game: The direct chemoselective nitrogenation of unactivated alkenes can be achieved through oxidative selenium catalysis (see scheme). This method provides a broad variety of allylic imides in yields of up to 89 % using N-fluorobenzenesulfonimide (NFSI) as the terminal oxidant and nitrogen source. Furthermore, an unprecedented selenium-catalyzed vinylic C(sp2)-H nitrogenation was discovered. Copyright

Taming the carboxyl group for directed carbometalation: Observations on the use of anions, dianions and ester enolates

Desrat, Sandy,Gray, Philip J.,Penny, Matthew R.,Motherwell, William B.

, p. 8918 - 8922 (2014/07/22)

Carboxylate anions, dianions and ester enolates provide simultaneous protection and activation for directed carbometalation reactions. Advantage can be taken of the bis-carbanionic character of the intermediate for further controlled C-C bond forming reac

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