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500-66-3

  • Product Name:Olivetol
  • Molecular Formula:C11H16O2
  • Appearance:light purple to brown crystalline mass
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Product Details

Appearance:light purple to brown crystalline mass

Purity:99%

Buy High Quality Pharmaceutical Grade Olivetol 500-66-3 In Stock

  • Molecular Formula:C11H16O2
  • Molecular Weight:180.247
  • Appearance/Colour:light purple to brown crystalline mass 
  • Vapor Pressure:0.000273mmHg at 25°C 
  • Melting Point:46-48 °C(lit.) 
  • Refractive Index:1.546 
  • Boiling Point:313.259 °C at 760 mmHg 
  • PKA:9.59±0.10(Predicted) 
  • Flash Point:148.758 °C 
  • PSA:40.46000 
  • Density:1.069 g/cm3 
  • LogP:2.83050 

High Purity Olivetol 500-66-3  In Medicine GMP Manufacturer In Bulk Supply, Fast Delivery

Olivetol (OLV), known as 3, 5-dihydroxypentylene, was a natural polyphenol compound that could be found in lichens, some insects, and many plants, is an important polyphenol compound and intermediate in the synthesis of cannabinoids possessing many types of biological activities. It is used in various methods to produce synthetic analogues of cannabinoids. Olivetol is one of the first intermediate involved in the cannabinoid biosynthesis in Cannabis sativa. OLV structure is found in cannabinoids, so OLV could be used as an analogue of CBD as it could mimic its interactions with the drug delivery systems.

InChI:InChI=1/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3

500-66-3 Relevant articles

Electrochemical Detection of Olivetol Based on Poly(L-Serine) Film Layered Copper Oxide Modified Carbon Paste Electrode (p-L-Serine/CuO/CPE)

Zongyi You ,Yi Zhang ,Shengwen Duan * and Liangliang Liu

Nanomaterials, 2022

To the best of our knowledge, there was a rare report of the electrochemical sensor based on CPE for the determination of olivetol. In this study, CuO nanoparticles and L-serine were modified on CPE, resulting in the p-L-serine/CuO/CPE for the sensitive detection of olivetol in the electrochemical method.

A catalytic, oxidative synthesis of olivetol, methyl olivetolate and orthogonally protected methyl ether derivatives

David Hurem , Benjamin J. Macphail , Rina Carlini , Jason Lewis , James McNulty

SynOpen, 2021

Olivetolic acid is thus a central intermediate in the biosynthesis of the phytocannabinoids, while olivetolic acid and more commonly olivetol are crucial building blocks in the chemical synthesis of phytocannabinoids and analogues. In conclusion, the synthesis of olivetolic acid methyl ester 3 has been achieved in 65% isolated yield in only two steps from the cyclic diketone 8 employing an oxidative aromatization strategy that is catalytic in iodine in DMSO.

500-66-3 Process route

methyl 6-n-pentyl-2-hydroxy-4-oxo-cyclohex-2-ene-1-carboxylate
27871-89-2

methyl 6-n-pentyl-2-hydroxy-4-oxo-cyclohex-2-ene-1-carboxylate

Olivetol
500-66-3

Olivetol

Conditions
Conditions Yield
With bromine; In N,N-dimethyl-formamide; at 160 ℃; for 10h; Cooling with ice;
69.3%
With bromine; In N,N-dimethyl-formamide; at 80 - 160 ℃;
69.3%
With bromine; In N,N-dimethyl-formamide; at 160 ℃; for 11.5h; Cooling with ice;
69.3%
With bromine; In N,N-dimethyl-formamide; at 160 ℃; for 10h; Cooling with ice;
69.3%
With bromine; In N,N-dimethyl-formamide; at 80 - 160 ℃; for 11.5h; Cooling with ice;
69.3%
3,5-diamino-1-pentylbenzene

3,5-diamino-1-pentylbenzene

Olivetol
500-66-3

Olivetol

Conditions
Conditions Yield
3,5-diamino-1-pentylbenzene; With sulfuric acid; sodium nitrite; In dichloromethane; at 5 ℃;
With sulfuric acid; sodium sulfate; In water; for 1h; Reflux;
78%

500-66-3 Upstream products

  • 67-56-1
    67-56-1

    methanol

  • 491-47-4
    491-47-4

    olivetoric acid

  • 64-18-6
    64-18-6

    formic acid

  • 22976-40-5
    22976-40-5

    1,3-dimethoxy-5-pentylbenzene

500-66-3 Downstream products

  • 855875-40-0
    855875-40-0

    2,4-dihydroxyl-6-pentylbenzaldehyde

  • 56661-19-9
    56661-19-9

    (+/-)-1-hydroxy-9-methyl-3-pentyl-7,8,9,10-tetrahydro-benzo[c]chromen-6-one

  • 18456-88-7
    18456-88-7

    5-Pentyl-1,3-cyclohexanedione

  • 78463-35-1
    78463-35-1

    4-bromo-5-pentylbenzene-1,3-diol