120577-01-7

Upstream product

• 97133-78-3 N-(cis-2-hydroxy-trans-3-phenoxycyclopentyl)acetamide 
• 251104-24-2 N₁-[(1S,2S,3S)-2-hydroxy-3-phenoxycyclopentyl]acetamide 
• 97133-77-2 cis-N-(6-oxabicyclo<3.1.0>hex-2-yl)acetamide 
• 139-02-6 sodium phenoxide 

Downstream Products

• 97133-70-5 cis-2-<(1-methylethyl)amino>-trans-5-phenoxycyclopentanol 
• 251104-28-6 (-)-N₂-[(1S,2S,3S)-2-hydroxy-3-phenoxycyclopentyl]-(2S)-2,3-dihydro-1,4-benzodioxine-2-carboxamide 
• 251104-27-5 (-)-N₂-[(1R,2R,3R)-2-hydroxy-3-phenoxycyclopentyl]-(2S)-2,3-dihydro-1,4-benzodioxine-2-carboxamide 
• 251104-25-3 (+)-N₂-[(1S,2S,3S)-2-hydroxy-3-phenoxycyclopentyl]-(2R)-2,3-dihydro-1,4-benzodioxine-2-carboxamide 
• 251104-26-4 (+)-N₂-[(1R,2R,3R)-2-hydroxy-3-phenoxycyclopentyl]-(2R)-2,3-dihydro-1,4-benzodioxine-2-carboxamide 

Relevant academic research and scientific papers

WB 4101-related compounds. 2. Role of the ethylene chain separating amine and phenoxy units on the affinity for α1-adrenoreceptor subtypes and 5-HT(1A) receptors

WB 4101 (1)-related benzodioxanes were synthesized by replacing the ethylene chain separating the amine and the phenoxy units of 1 with a cyclopentanol moiety, a feature of 6,7-dihydro-5-[[(cis-2-hydroxy-trans-3- phenoxycyclopentyl)amino]methyl]-2-methylb