87613-50-1

Basic information

• Product Name: Phenol, 3-(1,1-dimethylheptyl)-5-methoxy-
• CAS NO: 87613-50-1
• Molecular Formula: C16H26O2
• Molecular Weight: 250.381
• Mol File: 87613-50-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phenol, 3-(1,1-dimethylheptyl)-5-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3-(1,1-dimethylheptyl)-5-methoxy-(87613-50-1)
• EPA Substance Registry System: Phenol, 3-(1,1-dimethylheptyl)-5-methoxy-(87613-50-1)

Safety Data

• Hazardous Substances Data: 87613-50-1(Hazardous Substances Data)

Upstream product

• 60526-81-0 1-(1',1'-dimethylheptyl)-3,5-dimethoxybenzene 
• 866398-16-5 trifluoromethanesulfonic acid 4-(1,1-dimethylheptyl)-2,6-dimethoxyphenyl ester 
• 91-10-1 1,3-dimethoxy-2-hydroxy-benzene 
• 628-44-4 2-methyl-2-octanol 
• 60526-69-4 4-(1,1-dimethylheptyl)-2,6-dimethoxyphenol 

Downstream Products

• 866398-19-8 trifluoromethanesulfonic acid 3-(1,1-dimethylheptyl)-5-methoxyphenyl ester 
• 1025867-83-7 C₂₀H₃₅O₅P 
• 1026176-11-3 (1S,4R,5S)-4-[4-(1,1-Dimethyl-heptyl)-2-hydroxy-phenyl]-6,6-dimethyl-bicyclo[3.1.1]heptan-2-one 
• 181764-33-0 1-bromo-4-(1,1-dimethylheptyl)-2-methoxybenzene 
• 866398-21-2 1-(1,1-dimethylheptyl)-3-methoxybenzene 
• 83002-04-4 CP 55,940 
• 866398-07-4 (7R,8R)-7-[4-(1,1-dimethylheptyl)-2-methoxyphenyl]-8-(2-[1,3]dioxolan-2-ylethyl)-1,4-dioxaspiro[4,5]decane 
• 866398-09-6 3-{(7R,8R)-7-[4-(1,1-dimethylheptyl)-2-methoxyphenyl]-1,4-dioxaspiro[4,5]dec-8-yl}propan-1-ol 
• 866398-05-2 (1R,4R,5R,8S)-4-[4-(1,1-dimethylheptyl)-2-methoxyphenyl]-8-methoxymethoxybicyclo[3.3.1]non-3-en-2-one 
• 866398-11-0 (1R,3R,4R)-3-[4-(1,1-dimethylheptyl)-2-methoxyphenyl]-4-(3-hydroxypropyl)cyclohexanol 

Relevant articles and documents

Synthesis and pharmacology of a very potent cannabinoid lacking a phenolic hydroxyl with high affinity for the CB2 receptor

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Expedient synthesis of potent cannabinoid receptor agonist (-)-CP55,940

(Chemical Equation Presented) A stereocontrolled synthesis of (-)-CP55,940, a potent cannabinoid receptor agonist, has been attained using a novel aldolization/retroaldolization interconversion strategy, in which a temporarily generated chiral aldol motif plays essential roles.