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124167-85-7

1-phenyl-4,5-dimethyl-1E,5-hexadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124167-85-7 Structure

  • Basic information

    1. Product Name: 1-phenyl-4,5-dimethyl-1E,5-hexadiene
    2. Synonyms: 1-phenyl-4,5-dimethyl-1E,5-hexadiene
    3. CAS NO:124167-85-7
    4. Molecular Formula:
    5. Molecular Weight: 186.297
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124167-85-7.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-phenyl-4,5-dimethyl-1E,5-hexadiene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyl-4,5-dimethyl-1E,5-hexadiene(124167-85-7)
    11. EPA Substance Registry System: 1-phenyl-4,5-dimethyl-1E,5-hexadiene(124167-85-7)

  • 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: 124167-85-7(Hazardous Substances Data)

124167-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124167-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,1,6 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124167-85:
(8*1)+(7*2)+(6*4)+(5*1)+(4*6)+(3*7)+(2*8)+(1*5)=117
117 % 10 = 7
So 124167-85-7 is a valid CAS Registry Number.

124167-85-7Upstream product

124167-85-7Downstream Products

124167-85-7Relevant articles and documents

REACTIONS OF ?-ALLYL COMPLEXES OF Ti(III) WITH ALLYL, ALKYL, AND PROPARGYL ELECTROPHILES

Kasatkin, A. N.,Kulak, A. N.,Tolstikov, G. A.,Lomakina, S. I.

, p. 1875 - 1889 (2007/10/02)

The reactions of the ?-allyl complexes of Ti(III) with allyl bromides lead to the production of a mixture of cross-coupling and homocoupling products.In the case of alkyl and propargyl halides the dehalogenation products are formed.The reaction of the ?-allyl complexes of Ti(III) with allyl acetates, allyl phenyl ethers, and allyl aryl sulfones are catalyzed by Pd(PPh3)4 and give cross-coupling or elimination products, depending on the structure of the initial substrate.

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