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444310-19-4

(E)-ethyl 8-phenyloct-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 444310-19-4 Structure

  • Basic information

    1. Product Name: (E)-ethyl 8-phenyloct-2-enoate
    2. Synonyms: (E)-ethyl 8-phenyloct-2-enoate
    3. CAS NO:444310-19-4
    4. Molecular Formula:
    5. Molecular Weight: 246.349
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 444310-19-4.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: (E)-ethyl 8-phenyloct-2-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-ethyl 8-phenyloct-2-enoate(444310-19-4)
    11. EPA Substance Registry System: (E)-ethyl 8-phenyloct-2-enoate(444310-19-4)

  • 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: 444310-19-4(Hazardous Substances Data)

444310-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 444310-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,3,1 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 444310-19:
(8*4)+(7*4)+(6*4)+(5*3)+(4*1)+(3*0)+(2*1)+(1*9)=114
114 % 10 = 4
So 444310-19-4 is a valid CAS Registry Number.

444310-19-4Relevant articles and documents

Entry to β-alkoxyacrylates via gold-catalyzed intermolecular coupling of alkynoates and allylic ethers

Park, Sae Rom,Kim, Cheoljae,Kim, Dong-Gil,Thrimurtulu, Neetipalli,Yeom, Hyun-Suk,Jun, Jungho,Shin, Seunghoon,Rhee, Young Ho

, p. 1166 - 1169 (2013/05/09)

The first gold-catalyzed intermolecular coupling of alkynoates and allylic ethers invoking alkoxy addition and [3,3]-sigmatropic rearrangement as the key mechanism has been developed. Remarkably, the reaction showed complete chemoselectivity toward the pathway initiated by the alkoxy addition to alkynes. This unprecedented reactivity led to a new access to diversely substituted β-alkoxyacrylates in a highly efficient manner.

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