293756-94-2

Basic information

• Product Name: N-methyl-N-[2-(2,4,6-tribromo-3-hydroxy-phenyl)-ethyl]-formamide
• Synonyms: N-methyl-N-[2-(2,4,6-tribromo-3-hydroxy-phenyl)-ethyl]-formamide
• CAS NO: 293756-94-2
• Molecular Weight: 415.907
• Mol File: 293756-94-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-methyl-N-[2-(2,4,6-tribromo-3-hydroxy-phenyl)-ethyl]-formamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyl-N-[2-(2,4,6-tribromo-3-hydroxy-phenyl)-ethyl]-formamide(293756-94-2)
• EPA Substance Registry System: N-methyl-N-[2-(2,4,6-tribromo-3-hydroxy-phenyl)-ethyl]-formamide(293756-94-2)

Safety Data

• Hazardous Substances Data: 293756-94-2(Hazardous Substances Data)

Upstream product

• 220299-54-7 N-methyl-(3-hydroxyphenyl)acetamide 
• 51674-33-0 2-(3-Hydroxyphenyl)-methylaminoethane 
• 33543-62-3 2-(3-methoxyphenyl)-N-methylethan-1-amine 
• 42058-59-3 3-hydroxy-benzeneacetic acid, methyl ester 
• 18927-05-4 methyl (3-methoxyphenyl)acetate 
• 1798-09-0 m-methoxyphenylacetic acid 
• 52059-50-4 2-(3-hydroxyphenyl)ethyl bromide 
• 621-37-4 m-hydroxyphenylacetic acid 
• 2146-61-4 3-methoxyphenethyl bromide 
• 53102-68-4 N-methyl-(3-methoxyphenyl)acetamide 

Downstream Products

• 294210-58-5 lutamide C 

Relevant articles and documents

Synthesis and biological activities of the marine bryozoan alkaloids convolutamines A, C and F, and lutamides A and C

Synthesis of convolutamines and lutamides, new 2,4,6-tribromo-3-methoxyphenethylamine alkaloids isolated from Floridian marine bryozoan Amathia convoluta, was accomplished by a sequence of reactions starting from 3-hydroxyphenethylamines. Cytotoxities of the synthetic lutamides, convolutamines and their de-O-methyl derivatives were examined using drug-sensitive and -resistant P388 as well as KB cell lines. The bioassay suggests that the 2,4,6-tribromo-3-methoxyphenethylamine is an indispensable unit for detection of the activities. Additionally, a reversal of drug resistance by those alkaloids is recognized. Copyright (C) 2000 Elsevier Science Ltd.