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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](CAS/20200119/GIF/58940-28-6.gif) |
| | 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 | | pka | 9+-.0.45(Predicted) |
| WGK Germany | WGK 2 | | Storage Class | 3 - Flammable liquids | | Hazard Classifications | Acute Tox. 4 Dermal Acute Tox. 4 Inhalation Acute Tox. 4 Oral Eye Irrit. 2 Flam. Liq. 2 |
| | 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]. | | Definition | ChEBI: 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is a hydroxy-cannabidiol that is cannabidiol in which the 6-pro-S hydrogen of the cyclohexene ring has been replaced by a hydroxy group.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 |
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