214466-03-2

Basic information

• Product Name: (2S,3S)-3-(3,5-Dimethoxy-phenyl)-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-methyl-butan-1-one
• Synonyms: (2S,3S)-3-(3,5-Dimethoxy-phenyl)-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-methyl-butan-1-one
• CAS NO: 214466-03-2
• Molecular Weight: 435.585
• Mol File: 214466-03-2.mol

Chemical Properties

• CAS DataBase Reference: (2S,3S)-3-(3,5-Dimethoxy-phenyl)-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-methyl-butan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-3-(3,5-Dimethoxy-phenyl)-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-methyl-butan-1-one(214466-03-2)
• EPA Substance Registry System: (2S,3S)-3-(3,5-Dimethoxy-phenyl)-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-methyl-butan-1-one(214466-03-2)

Safety Data

• Hazardous Substances Data: 214466-03-2(Hazardous Substances Data)

Upstream product

• 214466-02-1 N-[(E)-2-methyl-3-{3,5-dimethoxyphenyl}-2-propenoyl]-bornane-10,2-sultam 

Downstream Products

• 214466-00-9 3'S-(3,5-dimethoxyphenyl)-2'S-methylbutanoic acid 
• 199388-20-0 3'S-(3,5-dimethoxyphenyl)-2'S-methyl-1-butanol 
• 14950-73-3 2'S-(3,5-dimethoxyphenyl)-3'R-methyloctane 
• 214770-69-1 5-((1S,2R)-1,2-Dimethyl-heptyl)-benzene-1,3-diol 
• 374559-49-6 Toluene-4-sulfonic acid (2S,3S)-3-(3,5-dimethoxy-phenyl)-2-methyl-butyl ester 

Relevant articles and documents

Enantioselective synthesis of 11-hydroxy-(1′S,2′R)-dimethylheptyl-Δ8-THC, a very potent CB1 agonist

An enantioselective synthesis of the (1S,2R)-dimethylheptyl cannabinoid side chain has been developed and employed in the synthesis of 11-hydroxy-(1′S,2′R)-dimethylheptyl-Δ8-THC, one of the most potent traditional cannabinoids known. The synthesis involves a highly stereoselective addition of dimethylcopperlithium to an enoyl sultam which incorporates Opplozer's auxiliary.

Enantioselective synthesis and pharmacology of 11-hydroxy-(1'S,2'R)- dimethylheptyl]-Δ8-THC

An enantioselective synthesis of the (1'S,2'R)-dimethylheptyl cannabinoid side chain has been developed and employed in the synthesis of 11-hydroxy-(1'S,2'R)-dimethylheptyl-Δ8-THC (3). Pharmacology, in vivo and in vitro, indicate (3) to be one of the most potent traditional cannabinoids known.