532400-25-2

Upstream product

• 532400-24-1 ((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-{(1R,2R)-2-[(R)-2-(4-phenyl-butyl)-2,3-dihydro-benzofuran-4-yl]-cyclopropyl}-methanone 
• 532400-23-0 (E)-1-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-[(R)-2-(4-phenyl-butyl)-2,3-dihydro-benzofuran-4-yl]-propenone 
• 532400-19-4 (E)-3-[2-((S)-2-Hydroxy-6-phenyl-hexyl)-3-methoxymethoxy-phenyl]-acrylic acid ethyl ester 
• 532400-20-7 ethyl (2E)-3-[2-((2S)-2-Hydroxy-6-Phenylhexyl)-3-hydroxyphenyl]-prop-2-enoate 
• 532400-21-8 (E)-3-[(R)-2-(4-Phenyl-butyl)-2,3-dihydro-benzofuran-4-yl]-acrylic acid ethyl ester 
• 532400-22-9 (E)-3-[(R)-2-(4-Phenyl-butyl)-2,3-dihydro-benzofuran-4-yl]-acrylic acid 
• 532400-18-3 (3S)-5-(Methoxymethoxy)-3-(4-phenylbutyl)isochroman-1-ol 
• 532400-17-2 (3S)-5-(Methoxymethoxy)-3-(4-phenylbutyl)isochroman-1-one 
• 863555-64-0 (S)-5-Methoxymethoxy-3-((E)-4-phenyl-but-3-enyl)-isochroman-1-one 
• 532400-14-9 (S)-3-(3-Hydroxy-propyl)-5-methoxymethoxy-isochroman-1-one 
• 532400-15-0 3-[(3S)-5-(Methoxymethoxy)-1-oxoisochroman-3-yl]propanal 
• 532399-61-4 (3S)-5-(Methoxymethoxy)-3-prop-2-enylisochroman-1-one 
• 532399-59-0 ethyl 3-(Methoxymethoxy)-2-prop-2-enylbenzoate 
• 532399-60-3 ethyl 3-(Methoxymethoxy)-2-(2-oxoethyl)benzoate 

Downstream Products

• 532399-55-6 1-Ethyl-3-{(1R,2R)-2-[(R)-2-(4-phenyl-butyl)-2,3-dihydro-benzofuran-4-yl]-cyclopropylmethyl}-urea 
• 532400-28-5 C-{(1R,2R)-2-[(R)-2-(4-Phenyl-butyl)-2,3-dihydro-benzofuran-4-yl]-cyclopropyl}-methylamine 
• 532400-27-4 (1R,2R)-2-[(R)-2-(4-Phenyl-butyl)-2,3-dihydro-benzofuran-4-yl]-cyclopropanecarbaldehyde oxime 
• 532400-26-3 (1R,2R)-2-[(R)-2-(4-Phenyl-butyl)-2,3-dihydro-benzofuran-4-yl]-cyclopropanecarbaldehyde 

Relevant academic research and scientific papers

(R)-2-(4-Phenylbutyl)dihydrobenzofuran derivatives as melatoninergic agents

(R)-2-(4-Phenylbutyl)dihydrobenzofuran derivatives (e.g., 3 and 4) were synthesized as novel melatoninergic ligands with significantly lower vasoconstrictive activity in vitro in the rat tail artery. Binding affinity assays were performed on cloned human