66384-48-3

Basic information

• Product Name: 2-(2-iodo-4,5-dimethoxyphenyl)ethan-1-amine
• Synonyms: 2-(2-iodo-4,5-dimethoxyphenyl)ethan-1-amine
• CAS NO: 66384-48-3
• Molecular Weight: 307.131
• Mol File: 66384-48-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-(2-iodo-4,5-dimethoxyphenyl)ethan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-iodo-4,5-dimethoxyphenyl)ethan-1-amine(66384-48-3)
• EPA Substance Registry System: 2-(2-iodo-4,5-dimethoxyphenyl)ethan-1-amine(66384-48-3)

Safety Data

• Hazardous Substances Data: 66384-48-3(Hazardous Substances Data)

Upstream product

• 58432-83-0 (4,5-dimethoxy-2-iodophenyl)methyl chloride 
• 14301-36-1 N-[2-(3,4-dimethoxyphenyl)ethyl]formamide 
• 1314098-76-4 N-(tert-butoxycarbonyl)-2-(2-iodo-4,5-dimethoxyphenyl)ethylamine 
• 98062-25-0 tert-butyl N-[2-(3,4-dimethoxyphenyl)ethyl]carbamate 
• 93-17-4 3,4-dimethoxyphenylacetonitrile 
• 58432-85-2 N-(2-iodo-4,5-dimethoxyphenethyl)formamide 
• 58432-84-1 2-(2-iodo-4,5-dimethoxyphenyl)acetonitrile 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 

Downstream Products

• 809233-38-3 1-[2-(2-iodo-4,5-dimethoxyphenyl)ethyl]octahydroindole-7a-carbonitrile 
• 809233-34-9 [2-(1,4-dioxaspiro[4.5]dec-6-yl)ethyl]-[2-(2-iodo-4,5-dimethoxyphenyl)ethyl]amine 
• 1314098-76-4 N-(tert-butoxycarbonyl)-2-(2-iodo-4,5-dimethoxyphenyl)ethylamine 
• 1607804-24-9 N-t-butoxycarbonyl-2-(2-iodo-4,5-dihydroxyphenyl)ethanamine 
• 1607804-00-1 2-(diacetoxyiodo)-1-[2-[(di-tert-butoxycarbonyl)amino]ethyl]-4,5-bis(ethoxymethoxy)benzene 
• 1607804-19-2 2-[2-[(di-tert-butoxycarbonyl)amino]ethyl]-4,5-bis(ethoxymethoxy)iodobenzene 
• 1607804-25-0 N-(t-butoxycarbonyl)-2-(2-iodo-4,5-bis(ethoxymethoxy)phenyl)ethanamine 
• 1384186-22-4 (2S,3R)-3-((tert-butyldimethylsilyl)oxy)-N-(2-iodo-4,5-dimethoxyphenethyl)-2-isobutylpent-4-enamide 
• 1384186-21-3 (2S,3R)-3-((tert-butyldimethylsilyl)oxy)-N-(4,5-dimethoxy-2-vinylphenethyl)-2-isobutylpent-4-enamide 
• 1228458-10-3 (2R,3S,11bR)-2-hydroxy-3-isobutyl-9,10-dimethoxy-2,3,6,7-tetrahydro-1H-pyrido[2,1-α]isoquinolin-4(11bH)-one 
• 1384186-29-1 C₄₀H₅₈N₂O₈ 
• 1228458-05-6 (5S,6R,E)-6-(tert-butyldimethylsilyloxy)-5-isobutyl-10,11-dimethoxy-2,3,5,6-tetrahydrobenzo[d]azecin-4(1H)-one 
• 1384186-23-5 C₅₂H₈₆N₂O₈Si₂ 
• 1026016-83-0 ((3R,11bR)-3-isobutyl-9.10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one) 

Relevant articles and documents

Synthesis and Biological Evaluation of Endocannabinoid Uptake Inhibitors Derived from WOBE437

WOBE437 ((2E,4E)-N-(3,4-dimethoxyphenethyl)dodeca-2,4-dienamide, 1) is a natural product-derived, highly potent inhibitor of endocannabinoid reuptake. In this study, we synthesized almost 80 analogues of 1 with different types of modifications in the dodecadienoyl domain as well as the dimethoxyphenylethyl head group, and we investigated their effects on anandamide uptake into U937 cells. Intriguingly, none of these analogues was a more potent inhibitor of anandamide uptake than WOBE437 (1). At the same time, a number of WOBE437 variants exhibited potencies in the sub-100 nM range, with high selectivity over inhibition of the endocannabinoid-degrading enzyme fatty acid amide hydrolase; two compounds were virtually equipotent with 1. Interestingly, profound activity differences were observed between analogues in which either of the two methoxy substituents in the head group had been replaced by the same bulkier alkoxy group. Some of the compounds described here could be interesting departure points for the development of potent endocannabinoid uptake inhibitors with more drug-like properties.

PROCESSES AND REAGENTS FOR MAKING DIARYLIODONIUM SALTS

This invention relates to processes and reagents for making diaryliodonium salts, which are useful for the preparation of fluorinated and radiofluorinated aromatic compounds.

An improved stereocontrolled route to cis-erythrinanes by combined intramolecular Strecker and Bruylants reaction

Condensation of (2-iodophenyl)ethylamines with cyclohexanoylacetaldehyde provided the corresponding aldimines which were reduced yielding secondary phenethylcyclohexanoylethylamines. These in turn were appropriate intermediates to prepare several erythrin