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CAS

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1059590-42-9

butyl (2E,4E,6E)-4,5-di(4-chlorophenyl)-7-phenyl-2,4,6-heptatrienoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1059590-42-9 Structure

  • Basic information

    1. Product Name: butyl (2E,4E,6E)-4,5-di(4-chlorophenyl)-7-phenyl-2,4,6-heptatrienoate
    2. Synonyms: butyl (2E,4E,6E)-4,5-di(4-chlorophenyl)-7-phenyl-2,4,6-heptatrienoate
    3. CAS NO:1059590-42-9
    4. Molecular Formula:
    5. Molecular Weight: 477.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1059590-42-9.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: butyl (2E,4E,6E)-4,5-di(4-chlorophenyl)-7-phenyl-2,4,6-heptatrienoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: butyl (2E,4E,6E)-4,5-di(4-chlorophenyl)-7-phenyl-2,4,6-heptatrienoate(1059590-42-9)
    11. EPA Substance Registry System: butyl (2E,4E,6E)-4,5-di(4-chlorophenyl)-7-phenyl-2,4,6-heptatrienoate(1059590-42-9)

  • 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: 1059590-42-9(Hazardous Substances Data)

1059590-42-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1059590-42-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,9,5,9 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1059590-42:
(9*1)+(8*0)+(7*5)+(6*9)+(5*5)+(4*9)+(3*0)+(2*4)+(1*2)=169
169 % 10 = 9
So 1059590-42-9 is a valid CAS Registry Number.

1059590-42-9Downstream Products

1059590-42-9Relevant articles and documents

Palladium-catalyzed intermolecular three-component coupling of organic halides with alkynes and alkenes: Efficient synthesis of oligoene compounds

Shibata, Kana,Satoh, Tetsuya,Miura, Masahiro

, p. 2317 - 2325 (2008/09/19)

The intermolecular three-component coupling of aryl or vinyl halides, diarylacetylenes, and monosubstituted alkenes effectively proceeds in the presence of palladium acetate, lithium chloride, and sodium bicarbonate as catalyst, promoter, and base, respectively, in aqueous DMF or DMSO to produce the corresponding 1,3-butadiene or 1,3,5-hexatriene derivatives. Use of dienyl bromides allows the coupling to afford 1,3,5,7-octatetraenes. Under the present catalytic conditions, fulvene derivatives are also formed efficiently by the 1:2 coupling of vinyl bromides and diarylacetylenes without adding the alkenes.

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