220169-81-3

Basic information

• Product Name: (S)-1-benzyloxy-5-(3,5-dimethoxyphenyl)-2-methylpent-4-yne
• Synonyms: (S)-1-benzyloxy-5-(3,5-dimethoxyphenyl)-2-methylpent-4-yne
• CAS NO: 220169-81-3
• Molecular Weight: 324.42
• Mol File: 220169-81-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-1-benzyloxy-5-(3,5-dimethoxyphenyl)-2-methylpent-4-yne(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-benzyloxy-5-(3,5-dimethoxyphenyl)-2-methylpent-4-yne(220169-81-3)
• EPA Substance Registry System: (S)-1-benzyloxy-5-(3,5-dimethoxyphenyl)-2-methylpent-4-yne(220169-81-3)

Safety Data

• Hazardous Substances Data: 220169-81-3(Hazardous Substances Data)

Upstream product

• 63930-47-2 (2R)-3-bromo-2-[(methylpropyloxy)methyl]benzene 
• 171290-52-1 1-Ethynyl-3,5-dimethoxy-benzene 

Downstream Products

• 220170-07-0 Toluene-4-sulfonic acid (S)-5-(3,5-dimethoxy-phenyl)-2-methyl-pentyl ester 
• 220170-08-1 5-((R)-4-Methyl-heptyl)-benzene-1,3-diol 
• 220169-85-7 (R)-1-(3,5-dimethoxyphenyl)-4-methylheptane 
• 220169-83-5 (S)-5-(3,5-dimethoxyphenyl)-2-methyl-1-pentanol 

Relevant articles and documents

Synthesis and pharmacology of the isomeric methylheptyl-Δ8-tetrahydrocannabinols

The synthesis of the 3-heptyl, and the eleven isomeric 3-methylheptyl-Δ8-tetrahydrocannabinols (3-7, R and S methyl epimers, and 8) has been carried out. The synthetic approach entailed the synthesis of substituted resorcinols, which were subjected to acid catalyzed condensation with trans-para-menthadienol to provide the Δ8-THC analogue. The 1'-, 2'- and 3'-methylheptyl analogues (3-5) are considerably more potent than Δ8-THC. The 4'-, 5'- and 6'-methylheptyl isomers (6-8) are approximately equal in potency to Δ8-THC. Copyright (C) 1998 Elsevier Science Ltd.