O,O-Dimethyl-cannabigerol

O,O-Dimethyl-cannabigerol Suppliers list
Company Name: Energy Chemical  
Tel: 021-58432009 400-005-6266
Email: marketing@energy-chemical.com
Products Intro: Product Name:O,O-Dimethyl-cannabigerol
CAS:29106-16-9
Purity:NULL Package:10mg;2.5mg;25mg;5mg Remarks:NULL
Company Name: Cayman Chemical Company  
Tel: (800) 364-9897
Email: cayman@caymanchem.com
Products Intro: Product Name:Cannabigerol dimethyl ether
CAS:29106-16-9
Company Name: Shanghai Hao Zhun Biological Technology Co., Ltd.  
Tel: 15800340161
Email: info@zzsrm.com
Products Intro: Product Name:O,O-Dimethyl-cannabigerol
CAS:29106-16-9
O,O-Dimethyl-cannabigerol Basic information
Product Name:O,O-Dimethyl-cannabigerol
Synonyms:O,O-Dimethyl-cannabigerol;Cannabigerol dimethyl ether;Benzene, 2-[(2E)-3,7-dimethyl-2,6-octadien-1-yl]-1,3-dimethoxy-5-pentyl-
CAS:29106-16-9
MF:C23H36O2
MW:344.53
EINECS:
Product Categories:
Mol File:29106-16-9.mol
O,O-Dimethyl-cannabigerol Structure
O,O-Dimethyl-cannabigerol Chemical Properties
Boiling point 452.0±33.0 °C(Predicted)
density 0.927±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 55 mg/mL (159.64 mM; Need ultrasonic)|
form Liquid
color Light yellow to yellow
Water Solubility Water : < 0.1 mg/mL (insoluble)
Safety Information
MSDS Information
O,O-Dimethyl-cannabigerol Usage And Synthesis
Biological ActivityO,O-Dimethyl-cannabigerol is a natural product from Cannabis sativa. O,O-Dimethyl-cannabigerol has an antibacterial effect on drug-resistant strains of Staphylococcus aureus (MIC ranging from 1 to 2 μg/mL)[1]. O,O-Dimethyl-cannabigerol is a nonpsychoactive constituent[2][3]. O,O-Dimethyl-cannabigerol (compound 1) inhibits KB cells growth with IC50s of 44.55 μM (MTT assay) and 69.4 μM (SRB assay)[2].O,O-Dimethyl-cannabigerol (0-100 μM; 48 hours) induces cell cytotoxic in NIH 3T3 fibroblasts, with CD50s of 60.46 μM (MTT assay) and 82.98 μM (SRB assay)[2].O,O-Dimethyl-cannabigerol shows antitumor efficacy against melanoma cells of a mouse’s skin with an IC50 of 31.3 μM[2].
References[1]. Appendino G, et al. Antibacterial cannabinoids from Cannabis sativa: a structure-activity study. J Nat Prod. 2008;71(8):1427-1430. [2]. Han DS, et al. Synthesis and cytotoxic effects of deoxy-tomentellin. Arch Pharm Res. 2000;23(2):121-127. [3]. Caprioglio D, et al. O-Methyl Phytocannabinoids: Semi-synthesis, Analysis in Cannabis Flowerheads, and Biological Activity. Planta Med. 2019;85(11-12):981-986.
O,O-Dimethyl-cannabigerol Preparation Products And Raw materials
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