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CAS

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82102-27-0

1-methoxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82102-27-0 Structure

  • Basic information

    1. Product Name: 1-methoxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]benzene
    2. Synonyms:
    3. CAS NO:82102-27-0
    4. Molecular Formula:
    5. Molecular Weight: 236.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82102-27-0.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: 1-methoxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-methoxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]benzene(82102-27-0)
    11. EPA Substance Registry System: 1-methoxy-3-[(1E,3E)-4-phenylbuta-1,3-dien-1-yl]benzene(82102-27-0)

  • 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: 82102-27-0(Hazardous Substances Data)

82102-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82102-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,0 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82102-27:
(7*8)+(6*2)+(5*1)+(4*0)+(3*2)+(2*2)+(1*7)=90
90 % 10 = 0
So 82102-27-0 is a valid CAS Registry Number.

82102-27-0Relevant articles and documents

Stereoselective peterson olefinations from bench-stable reagents and N-phenyl imines

Das, Manas,Manvar, Atul,Jacolot, Ma?wenn,Blangetti, Marco,Jones, Roderick C.,O'Shea, Donal F.

, p. 8737 - 8740 (2015/06/08)

The synthesis of bench-stable α,α-bis(trimethylsilyl)toluenes and tris(trimethylsilyl)methane is described and their use in stereoselective Peterson olefinations has been achieved with a wide substrate scope. Product stereoselectivity was poor with carbonyl electrophiles (E/Z ～1:1 to 4:1) though this was significantly improved by employing the corresponding substituted N-benzylideneaniline (up to 99:1) as an alternative electrophile. The olefination byproduct was identified as N,N-bis(trimethylsilyl)aniline and could be easily separated from product by aqueous acid extraction. Evidence for an autocatalytic cycle has been obtained.

Reaction of trans,trans-1,4-Diphenylbutadiene and Maleic Anhydride. Substituent and Solvent Effects

Ballistreri, Francesco P.,Maccarone, Emanuele,Perrini, Giancarlo,Tomaselli, Gaetano A.,Torre, Michele

, p. 273 - 278 (2007/10/02)

Diels-Alder adducts from X-substituted diphenylbutadienes (X=p-NMe2, p-OMe, p-Me, m-OMe, H, p-Cl, m-Cl, p-CN, and m-NO2) and maleic anhydride, and from diphenylbutadiene and some dienophiles (N-methylmaleimide, N-phenylmaleimide, and 1,4-benzoquinone), ha

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