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CAS

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1384085-47-5

(S,E)-2-methyl-1-phenylhept-1-en-3-yl acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1384085-47-5 Structure

  • Basic information

    1. Product Name: (S,E)-2-methyl-1-phenylhept-1-en-3-yl acrylate
    2. Synonyms: (S,E)-2-methyl-1-phenylhept-1-en-3-yl acrylate
    3. CAS NO:1384085-47-5
    4. Molecular Formula:
    5. Molecular Weight: 258.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1384085-47-5.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: (S,E)-2-methyl-1-phenylhept-1-en-3-yl acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S,E)-2-methyl-1-phenylhept-1-en-3-yl acrylate(1384085-47-5)
    11. EPA Substance Registry System: (S,E)-2-methyl-1-phenylhept-1-en-3-yl acrylate(1384085-47-5)

  • 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: 1384085-47-5(Hazardous Substances Data)

1384085-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384085-47-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,0,8 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1384085-47:
(9*1)+(8*3)+(7*8)+(6*4)+(5*0)+(4*8)+(3*5)+(2*4)+(1*7)=175
175 % 10 = 5
So 1384085-47-5 is a valid CAS Registry Number.

1384085-47-5Downstream Products

1384085-47-5Relevant articles and documents

Synthetic approach toward cis-disubstituted γ- And δ-lactones through enantioselective dialkylzinc addition to aldehydes: Application to the synthesis of optically active flavors and fragrances

Pisani, Laura,Superchi, Stefano,D'Elia, Alessandra,Scafato, Patrizia,Rosini, Carlo

, p. 5779 - 5784 (2012/09/08)

A versatile and straightforward approach to optically active cis-4,5-disubstituted γ- and δ-lactones by catalytic enantioselective addition of dialkyzincs to cinnamic aldehydes and RCM ring closure has been reported. The synthetic importance of the enantioselective dialkylzinc alkylation of aldehydes has been thus widened. Such an approach has then been employed for the enantioselective synthesis of naturally occurring γ-lactone flavors like (S)-5-ethyl-butanolide (6a) and (4S,5S)-cis-whisky lactone (6b) and extended to the preparation of δ-lactones like (5S,6S)-5-methyl-6-ethylpentanolide (9a), precursor of the pheromone serricornin.

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