22703-18-0

Basic information

• Product Name: cannabidiol
• Synonyms: cannabidiol
• CAS NO: 22703-18-0
• Molecular Weight: 314.468
• Mol File: 22703-18-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: cannabidiol(CAS DataBase Reference)
• NIST Chemistry Reference: cannabidiol(22703-18-0)
• EPA Substance Registry System: cannabidiol(22703-18-0)

Safety Data

• Hazardous Substances Data: 22703-18-0(Hazardous Substances Data)

Upstream product

• 491-05-4 (+)-cis/trans-p-mentha-2,8-dien-1-ol 
• 500-66-3 Olivetol 
• 5392-40-5 (E/Z)-3,7-dimethyl-2,6-octadienal 
• 3411-09-4 2.6-Dimethoxy-4-pentyl-benzalaceton 
• 22976-40-5 1,3-dimethoxy-5-pentylbenzene 
• 7663-54-9 1-(2',6'-Dimethoxy-4'-n-pentylphenyl)-3-methyl-butadien 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 78-94-4 methyl vinyl ketone 
• 1242-67-7 1,3-dimethoxy-2-((1RS,6RS)-3-methyl-6-(prop-1-en-2-yl)cyclohex-2-enyl)-5-pentylbenzene 
• 141-27-5 3,7-dimethyl-2,6-octadienal 
• 38862-65-6 2,4-dihydroxy-6-n-pentylbenzoic acid ethyl ester 
• 945-51-7 1,1'-sulfinylbisbenzene 
• 139-66-2 diphenyl sulfide 
• 22771-44-4 (+)-p-mentha-2,8-dien-1-ol 

Downstream Products

• 43009-38-7 (6aS,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol 
• 16849-50-6 tetrahydrocannabinol 
• 14132-18-4 6,6,9-Trimethyl-3-pentyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromen-1-ol 
• 6909-05-3 iso-Δ⁸-tetrahydrocannabinol 
• 112639-17-5 Acetic acid 3-acetoxy-6-iodo-2-((R)-6-isopropenyl-3-methyl-cyclohex-2-enyl)-5-pentyl-phenyl ester 
• 40525-15-3 cannabidiol diacetate 

Relevant articles and documents

Process for production of delta-9- tetrahydrocannabinol

The present invention relates to a process for preparation of a delta-9-tetrahydrocannabinol compound or derivative thereof involving treating a first intermediate compound with an organoaluminum-based Lewis acid catalyst, under conditions effective to produce the delta-9-tetrahydrocannabinol compound or derivative thereof. Another aspect of the present invention relates to a process for preparation of a cannabidiol or cannabidiolate compound involving reacting a first starting compound with a second starting compound in the presence of a metal triflate catalyst, under conditions effective to form the cannabidiol or cannabidiolate compound. The present invention also relates to a compound of the formula: where R8, R9, and R10 are the same or different and independently selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, or halo, with R1, R2, and R3 defined herein.

BORON TRIFLUORIDE ETHERATE ON ALUMINA - A MODIFIED LEWIS ACID REAGENT. AN IMPROVED SYNTHESIS OF CANNABIDIOL.

Boron trifluoride etherate on alumina catalyses the condensation of resorcinols and monomethyl resorcinols with several monoterpenoid allylic alcohols: in contrast to paralell reactions with boron trifluoride etherate in solution the products obtained do not undergo further cyclisations.