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1578259-16-1

(E)-4-(2,5-dimethoxyphenyl)but-3-en-2-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1578259-16-1 Structure

  • Basic information

    1. Product Name: (E)-4-(2,5-dimethoxyphenyl)but-3-en-2-yl acetate
    2. Synonyms:
    3. CAS NO:1578259-16-1
    4. Molecular Formula:
    5. Molecular Weight: 250.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1578259-16-1.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)-4-(2,5-dimethoxyphenyl)but-3-en-2-yl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-(2,5-dimethoxyphenyl)but-3-en-2-yl acetate(1578259-16-1)
    11. EPA Substance Registry System: (E)-4-(2,5-dimethoxyphenyl)but-3-en-2-yl acetate(1578259-16-1)

  • 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: 1578259-16-1(Hazardous Substances Data)

1578259-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1578259-16-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,8,2,5 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1578259-16:
(9*1)+(8*5)+(7*7)+(6*8)+(5*2)+(4*5)+(3*9)+(2*1)+(1*6)=211
211 % 10 = 1
So 1578259-16-1 is a valid CAS Registry Number.

1578259-16-1Downstream Products

1578259-16-1Relevant articles and documents

Access to cinnamyl derivatives from arenes and allyl esters by a biomimetic aerobic oxidative dehydrogenative coupling

Gigant, Nicolas,Baeckvall, Jan-E.

, p. 1664 - 1667 (2014)

An efficient biomimetic aerobic oxidative dehydrogenative alkenylation of arenes with allyl esters is presented. The reaction proceeds under an ambient pressure of oxygen with relatively low catalyst loading of palladium acetate, employing catalytic amounts of electron-transfer mediators (ETMs). This study represents a new environmentally friendly method for the synthesis of cinnamyl derivatives.

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