1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-

1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl- Suppliers list
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1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl- Basic information
Product Name:1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-
Synonyms:1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-;6α-Hydroxycannabidiol;6α-Hydroxycannabidiol (1.0mg/ml in Acetonitrile);(?)-6α-hydroxy Cannabidiol;6a-Hydroxycannabidiol;(1'R,2'R,4'S)-5'-methyl-4-pentyl-2'-(prop-1-en-2-yl)-1',2',3',4'-tetrahydro-[1,1'-biphenyl]-2,4',6-triol;6-Hydroxy cannabidiol (6-OH-CBD) solution
CAS:58940-28-6
MF:C21H30O3
MW:330.46
EINECS:
Product Categories:
Mol File:58940-28-6.mol
1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl- Structure
1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl- Chemical Properties
Boiling point 506.5±50.0 °C(Predicted)
density 1.088±0.06 g/cm3(Predicted)
storage temp. -10 to -25°C
solubility DMF: 50 mg/ml; DMSO: 60 mg/ml; DMSO:PBS (pH 7.2) (1:3): 0.25 mg/ml; Ethanol: 35 mg/ml
form A crystalline solid
pka9+-.0.45(Predicted)
Safety Information
WGK Germany WGK 2
Storage Class3 - Flammable liquids
Hazard ClassificationsAcute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Flam. Liq. 2
MSDS Information
1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl- Usage And Synthesis
Uses(-)-6α-Hydroxy cannabidiol is a metabolite of Cannabidiol[1].
DefinitionChEBI: 6alpha-hydroxycannabidiol is a hydroxy-cannabidiol that is cannabidiol in which the 6-pro-S hydrogen of the cyclohexene ring has been replaced by a hydroxy group. It is one of the main metabolites of cannabidiol by human liver microsomes, produced by CYP2C19 and CYP3A. It has a role as a human xenobiotic metabolite. It is a hydroxy-cannabidiol, a member of resorcinols, an olefinic compound and a secondary alcohol.
References[1] Jiang R, et al. Identification of cytochrome P450 enzymes responsible for metabolism of cannabidiol by human liver microsomes. Life Sci. 2011 Aug 1;89(5-6):165-70. DOI:10.1016/j.lfs.2011.05.018
1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl- Preparation Products And Raw materials
Tag:1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-(58940-28-6) Related Product Information
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