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CAS

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1333071-61-6

4-[(E)-hexa-1,5-dienyl]-N,N-dimethylbenzenamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1333071-61-6 Structure

  • Basic information

    1. Product Name: 4-[(E)-hexa-1,5-dienyl]-N,N-dimethylbenzenamine
    2. Synonyms: 4-[(E)-hexa-1,5-dienyl]-N,N-dimethylbenzenamine
    3. CAS NO:1333071-61-6
    4. Molecular Formula:
    5. Molecular Weight: 201.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1333071-61-6.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: 4-[(E)-hexa-1,5-dienyl]-N,N-dimethylbenzenamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[(E)-hexa-1,5-dienyl]-N,N-dimethylbenzenamine(1333071-61-6)
    11. EPA Substance Registry System: 4-[(E)-hexa-1,5-dienyl]-N,N-dimethylbenzenamine(1333071-61-6)

  • 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: 1333071-61-6(Hazardous Substances Data)

1333071-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333071-61-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,0,7 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1333071-61:
(9*1)+(8*3)+(7*3)+(6*3)+(5*0)+(4*7)+(3*1)+(2*6)+(1*1)=116
116 % 10 = 6
So 1333071-61-6 is a valid CAS Registry Number.

1333071-61-6Downstream Products

1333071-61-6Relevant articles and documents

Catalytic intermolecular allyl-allyl cross-couplings between alcohols and boronates

Jimenez-Aquino, Agustin,Ferrer Flegeau, Emmanuel,Schneider, Uwe,Kobayashi, Shu

, p. 9456 - 9458 (2011)

We developed catalytic intermolecular C(sp3)-C(sp3) cross-couplings between various allyl alcohols and allyl boronates, which proceeded smoothly in the presence of nickel(0) under mild conditions to form 1,5-dienes with excellent linear- and γ-selectivity; the use of boronates proved to be crucial in terms of reactivity.

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