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CAS

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485805-43-4

Benzene, 1-methoxy-3-[(1E)-2-(2,6,6-trimethyl-2-cyclohexen-1-yl)ethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 485805-43-4 Structure

  • Basic information

    1. Product Name: Benzene, 1-methoxy-3-[(1E)-2-(2,6,6-trimethyl-2-cyclohexen-1-yl)ethenyl]-
    2. Synonyms:
    3. CAS NO:485805-43-4
    4. Molecular Formula: C18H24O
    5. Molecular Weight: 256.388
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 485805-43-4.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: Benzene, 1-methoxy-3-[(1E)-2-(2,6,6-trimethyl-2-cyclohexen-1-yl)ethenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1-methoxy-3-[(1E)-2-(2,6,6-trimethyl-2-cyclohexen-1-yl)ethenyl]-(485805-43-4)
    11. EPA Substance Registry System: Benzene, 1-methoxy-3-[(1E)-2-(2,6,6-trimethyl-2-cyclohexen-1-yl)ethenyl]-(485805-43-4)

  • 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: 485805-43-4(Hazardous Substances Data)

485805-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 485805-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,5,8,0 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 485805-43:
(8*4)+(7*8)+(6*5)+(5*8)+(4*0)+(3*5)+(2*4)+(1*3)=184
184 % 10 = 4
So 485805-43-4 is a valid CAS Registry Number.

485805-43-4Relevant articles and documents

First total synthesis of an analogue of montbretyl 12-methyl ether

Zhang, Cheng-Lu,Qiu, Ye-Hong,Pan, Xin-Fu

, p. 232 - 233 (2007/10/03)

The first total synthesis of the title compound 1 was accomplished starting from α-cyclocitral and benzyl triphenylphosphonium chloride 3 in seven steps via a strategy of AC→ABC. In the synthesis, t-BuOK/t-BuOH system was utilised for enolisation and the iso-propyl group was introduced in the last step.

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