Cannabidiol

Base Information Edit

Chemical Name:Cannabidiol
CAS No.:13956-29-1
Deprecated CAS:35542-48-4,18436-46-9,20547-66-4,521-37-9
Molecular Formula:C21H30 O2
Molecular Weight:314.468
Hs Code.:
European Community (EC) Number:689-176-3
UNII:19GBJ60SN5
DSSTox Substance ID:DTXSID00871959,DTXSID301038839
Nikkaji Number:J10.356J
Wikipedia:Cannabidiol
Wikidata:Q422917
NCI Thesaurus Code:C118452
RXCUI:2045371
Pharos Ligand ID:MFUZD2HFWKAA
Metabolomics Workbench ID:152117
ChEMBL ID:CHEMBL190461
Mol file:13956-29-1.mol

Synonyms:1,3-Benzenediol, 2-(3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl)-5-pentyl-, (1R-trans)-;Cannabidiol;Epidiolex

This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of Cannabidiol Edit

Chemical Property:

Vapor Pressure:3.14E-09mmHg at 25°C
Melting Point:62-63°C
Refractive Index:nD20 1.5404
Boiling Point:463.9 °C at 760 mmHg
Flash Point:206.3 °C
PSA：40.46000
Density:1.025 g/cm³
LogP:5.84650
Storage Temp.:2-8°C
XLogP3:6.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:314.224580195
Heavy Atom Count:23
Complexity:414

Purity/Quality:

Safty Information:

Pictogram(s): FT
Hazard Codes:F,T
Statements: 11-23/24/25-39/23/24/25
Safety Statements: 36/37-45-16-7

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Drug Classes:Anticonvulsants
Canonical SMILES:CCCCCC1=CC(=C(C(=C1)O)C2C=C(CCC2C(=C)C)C)O
Isomeric SMILES:CCCCCC1=CC(=C(C(=C1)O)[C@@H]2C=C(CC[C@H]2C(=C)C)C)O
Recent ClinicalTrials:Cannabidiol for Bipolar Depression (CBD-BD)
Recent EU Clinical Trials:Pilot study on the effect of cannabinoids THC + CBD on resistant spasticity in patients with chronic spinal cord injury.
Description Cannabidiol (CRM) (Item No. ISO60156) is a certified reference material categorized as a phytocannabinoid. Unlike Δ9-THC (Item Nos. ISO60157 | 12068), cannabidiol is non-psychoactive. This product is intended for research and forensic applications.
Uses Major non-psychoactive constituent of Cannabis. Exhibits multiple bioactivities including anticonvulsant, anxiolytic and anti-inflammatory effects. The (+)-isomers were more active than the (-)-isomers.

Technology Process of Cannabidiol

There total 129 articles about Cannabidiol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

(1′R,2′R)-5′-methyl-4-pentyl-2′-(prop-1-en-2-yl)-1′,2′,3′,4′-tetrahydro-[1,1′-biphenyl]-2,6-diyl bis(2,2-dimethylpropanoate): (1′R,2′R)-5′-methyl-4-pentyl-2′-(prop-1-en-2-yl)-1′,2′,3′,4′-tetrahydro-[1,1′-biphenyl]-2,6-diyl bis(2,2-dimethylpropanoate)

: 13956-29-1,521-37-9
CBD

Guidance literature:: With methylmagnesium bromide; In diethyl ether; toluene; at 110 ℃; for 12h; Solvent; Reagent/catalyst; Temperature; Inert atmosphere;
DOI:10.1021/acs.joc.9b02880