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1569083-76-6

(E)-methyl 2-(acetoxymethyl)-5-phenylpent-2-en-4-ynoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1569083-76-6 Structure

  • Basic information

    1. Product Name: (E)-methyl 2-(acetoxymethyl)-5-phenylpent-2-en-4-ynoate
    2. Synonyms: (E)-methyl 2-(acetoxymethyl)-5-phenylpent-2-en-4-ynoate
    3. CAS NO:1569083-76-6
    4. Molecular Formula:
    5. Molecular Weight: 258.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1569083-76-6.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)-methyl 2-(acetoxymethyl)-5-phenylpent-2-en-4-ynoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-methyl 2-(acetoxymethyl)-5-phenylpent-2-en-4-ynoate(1569083-76-6)
    11. EPA Substance Registry System: (E)-methyl 2-(acetoxymethyl)-5-phenylpent-2-en-4-ynoate(1569083-76-6)

  • 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: 1569083-76-6(Hazardous Substances Data)

1569083-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569083-76-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,0,8 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1569083-76:
(9*1)+(8*5)+(7*6)+(6*9)+(5*0)+(4*8)+(3*3)+(2*7)+(1*6)=206
206 % 10 = 6
So 1569083-76-6 is a valid CAS Registry Number.

1569083-76-6Upstream product

1569083-76-6Relevant articles and documents

Synthesis of substituted 3-furanoates from MBH-acetates of acetylenic aldehydes via tandem isomerization-deacetylation-cycloisomerization: Access to Elliott's alcohol

Reddy, Chada Raji,Krishna, Gaddam,Reddy, Motatipally Damoder

, p. 1664 - 1670 (2014/03/21)

A new method for the synthesis of 5-substituted furan-3-carboxylates from Morita-Baylis-Hillman acetates of acetylenic aldehydes is reported. The process involves palladium-catalyzed isomerization followed by base-promoted deacetylation and cycloisomerization reactions. The utility of this chemistry is further demonstrated by the synthesis of Elliott's alcohol, a key intermediate of the pyrethroid resmethrins. This journal is The Royal Society of Chemistry 2014.

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