63953-93-5

Basic information

• Product Name: Benzoic acid, 3-(3,7-dimethyl-2,6-octadienyl)-2,4-dihydroxy-6-pentyl-, methyl ester, (E)-
• CAS NO: 63953-93-5
• Molecular Formula: C23H34O4
• Molecular Weight: 374.521
• Mol File: 63953-93-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3-(3,7-dimethyl-2,6-octadienyl)-2,4-dihydroxy-6-pentyl-, methyl ester, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-(3,7-dimethyl-2,6-octadienyl)-2,4-dihydroxy-6-pentyl-, methyl ester, (E)-(63953-93-5)
• EPA Substance Registry System: Benzoic acid, 3-(3,7-dimethyl-2,6-octadienyl)-2,4-dihydroxy-6-pentyl-, methyl ester, (E)-(63953-93-5)

Safety Data

• Hazardous Substances Data: 63953-93-5(Hazardous Substances Data)

Upstream product

• 25654-31-3 2-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-pentyl-benzene-1,3-diol 
• 58016-28-7 methyl 2,6-dihydroxy-6-pentylbenzoate 
• 5392-40-5 (E/Z)-3,7-dimethyl-2,6-octadienal 
• 106-24-1 Geraniol 
• 67-56-1 methanol 
• 25555-57-1 CBGA 

Downstream Products

• 25555-57-1 CBGA 
• 25654-31-3 2-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-pentyl-benzene-1,3-diol 

Relevant articles and documents

CANNABINOID ACID ESTER COMPOSITIONS AND USES THEREOF

The present disclosure provides pharmaceutical compositions including a cannabinoid acid ester compound alone or in combination with one or more additional cannabinoid compounds. In some embodiments, the cannabinoid acid ester compound is a tetrahydrocann

SYNTHESIS OF PHYTOCANNABINOIDS INCLUDING A DECARBOXYLATION STEP

method for decarboxylating a carboxylated phytocannabinoid compound of Formula I to form a phytocannabinoid compound of Formula II: Formula I Formula II wherein: R1 is selected from the group consisting of: substituted or unsubstituted C1-C5 alkyl; R2 is selected from the group consisting of: OH or O, and R3 is selected from the group consisting of: a substituted or unsubstituted cyclohexene, a substituted or unsubstituted C2-C8 alkene, or a substituted or unsubstituted C2-C8 dialkene; or R2 is O, and R2 and R3 together form a ring structure in which R2 is an internal ring atom; wherein the method includes heating a reaction mixture comprising the carboxylated phytocannabinoid compound and a polar aprotic solvent in the presence of a LiCl for a time sufficient to decarboxylate at least a portion of the carboxylated phytocannabinoid compounds and form the phytocannabinoid compound.