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1263002-09-0

3-(4,4-dimethylcyclohexa-1,5-dienyl)furan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1263002-09-0 Structure

  • Basic information

    1. Product Name: 3-(4,4-dimethylcyclohexa-1,5-dienyl)furan
    2. Synonyms: 3-(4,4-dimethylcyclohexa-1,5-dienyl)furan
    3. CAS NO:1263002-09-0
    4. Molecular Formula:
    5. Molecular Weight: 174.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1263002-09-0.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: 3-(4,4-dimethylcyclohexa-1,5-dienyl)furan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4,4-dimethylcyclohexa-1,5-dienyl)furan(1263002-09-0)
    11. EPA Substance Registry System: 3-(4,4-dimethylcyclohexa-1,5-dienyl)furan(1263002-09-0)

  • 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: 1263002-09-0(Hazardous Substances Data)

1263002-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1263002-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,0,0 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1263002-09:
(9*1)+(8*2)+(7*6)+(6*3)+(5*0)+(4*0)+(3*2)+(2*0)+(1*9)=100
100 % 10 = 0
So 1263002-09-0 is a valid CAS Registry Number.

1263002-09-0Downstream Products

1263002-09-0Relevant articles and documents

Synthesis of dienes by palladium-catalyzed couplings of tosylhydrazones with aryl and alkenyl halides

Barluenga, Jose,Tomas-Gamasa, Maria,Aznar, Fernando,Valdes, Carlos

supporting information; experimental part, p. 3235 - 3240 (2011/02/28)

Two different combinations of coupling partners can be employed for the synthesis of conjugated dienes by palladium-catalyzed cross-coupling with tosylhydrazones: α,β-unsaturated ketone and aryl halide or alkenyl halide and non-conjugated tosylhydrazone. Depending on the substrate, a vinylogous hydride elimination is responsible for the formation of the final dienes. Copyright

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