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130472-33-2

1-(3,5-dimethoxyphenyl)oct-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130472-33-2 Structure

  • Basic information

    1. Product Name: 1-(3,5-dimethoxyphenyl)oct-1-ene
    2. Synonyms:
    3. CAS NO:130472-33-2
    4. Molecular Formula:
    5. Molecular Weight: 248.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130472-33-2.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-(3,5-dimethoxyphenyl)oct-1-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3,5-dimethoxyphenyl)oct-1-ene(130472-33-2)
    11. EPA Substance Registry System: 1-(3,5-dimethoxyphenyl)oct-1-ene(130472-33-2)

  • 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: 130472-33-2(Hazardous Substances Data)

130472-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130472-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,7 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130472-33:
(8*1)+(7*3)+(6*0)+(5*4)+(4*7)+(3*2)+(2*3)+(1*3)=92
92 % 10 = 2
So 130472-33-2 is a valid CAS Registry Number.

130472-33-2Downstream Products

130472-33-2Relevant articles and documents

Using (+)-carvone to access novel derivatives of (+)-ent-cannabidiol: The first asymmetric syntheses of (+)-ent-CBDP and (+)-ent-CBDV

Golliher, Alexandra E.,Tenorio, Antonio J.,Dimauro, Nina O.,Mairata, Nicolas R.,Holguin, F. Omar,Maio, William

, (2021)

(?)-Cannabidiol [(?)-CBD] has recently gained prominence as a treatment for neuro-inflammation and other neurodegenerative disorders; interest is also developing in its synthetic enantiomer, (+)-CBD, which has a higher affinity to CB1/CB2 receptors than the natural stereoisomer. We have developed an inexpensive, stereoselective route to access ent-CBD derivatives using (+)-carvone as a starting material. In addition to (+)-CBD, we report the first syntheses of (+)-cannabidivarin, (+)-cannabidiphorol as well as C-6/C-8 homologues.

Synthesis of 4,4-Disubstituted Cyclohexenones. Part 2. Cycloaddition of 2-Chloroacrylonitrile to 5-Substituted 1,3-Dimethoxycyclohexa-1,4-dienes

Clark, Richard S. J.,Holmes, Andrew B.,Matassa, Victor G.

, p. 1389 - 1400 (2007/10/02)

The cycloaddition of 2-chloroacrylonitrile to 1,3-dimethoxycyclohexadienes (3; R1=OMe, R2=H), derived by in situ conjugation of the Birch reduction products (12) produced from aromatic precursors (11) gave after acid work-up mainly bicyclooctanone

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