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2-[(E)-3,7-Dimethyl-2,6-octadienyl]-3-methoxy-5-pentylphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29106-17-0 Structure
  • Basic information

    1. Product Name: 2-[(E)-3,7-Dimethyl-2,6-octadienyl]-3-methoxy-5-pentylphenol
    2. Synonyms: 2-[(2E)-3,7-Dimethyl-2,6-octadienyl]-3-methoxy-5-pentylphenol;2-[(E)-3,7-Dimethyl-2,6-octadienyl]-3-methoxy-5-pentylphenol;Cannabigerol methyl ether;O-Methylcannabigerol
    3. CAS NO:29106-17-0
    4. Molecular Formula: C22H34O2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29106-17-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[(E)-3,7-Dimethyl-2,6-octadienyl]-3-methoxy-5-pentylphenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(E)-3,7-Dimethyl-2,6-octadienyl]-3-methoxy-5-pentylphenol(29106-17-0)
    11. EPA Substance Registry System: 2-[(E)-3,7-Dimethyl-2,6-octadienyl]-3-methoxy-5-pentylphenol(29106-17-0)
  • 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: 29106-17-0(Hazardous Substances Data)

29106-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29106-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,0 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29106-17:
(7*2)+(6*9)+(5*1)+(4*0)+(3*6)+(2*1)+(1*7)=100
100 % 10 = 0
So 29106-17-0 is a valid CAS Registry Number.

29106-17-0Relevant articles and documents

O-Methyl Phytocannabinoids: Semi-synthesis, Analysis in Cannabis Flowerheads, and Biological Activity

Caprioglio, Diego,Allegrone, Gianna,Pollastro, Federica,Valera, Stefano,Lopatriello, Annalisa,Collado, Juan A.,Munoz, Eduardo,Appendino, Giovanni,Taglialatela-Scafati, Orazio

, p. 981 - 986 (2019/08/20)

A general protocol for the selective mono-O-methylation of resorcinyl phytocannabinoids was developed. The availability of semisynthetic monomethyl analogues of cannabigerol, cannabidiol, and cannabidivarin (1a-3a, respectively) made it possible to quanti

Base-catalysed Double-bond Isomerizations of Cannabinoids: Structural and Stereochemical Aspects

Srebnik, Morris,Lander, Naphtali,Breuer, Aviva,Mechoulam, Raphael

, p. 2881 - 2886 (2007/10/02)

Base-catalysed double-bond isomerization offers a convenient, high-yield route to a variety of new cannabinoids, as well as to compounds of this group which are accessible with some difficulty.By this route we have obtained optically active Δ2-

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