201486-60-4

Basic information

• Product Name: 1-Indol-1-yl-4-(4-methoxy-phenoxy)-butan-1-ol
• Synonyms: 1-Indol-1-yl-4-(4-methoxy-phenoxy)-butan-1-ol
• CAS NO: 201486-60-4
• Molecular Weight: 311.381
• Mol File: 201486-60-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Indol-1-yl-4-(4-methoxy-phenoxy)-butan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Indol-1-yl-4-(4-methoxy-phenoxy)-butan-1-ol(201486-60-4)
• EPA Substance Registry System: 1-Indol-1-yl-4-(4-methoxy-phenoxy)-butan-1-ol(201486-60-4)

Safety Data

• Hazardous Substances Data: 201486-60-4(Hazardous Substances Data)

Upstream product

• 88-72-2 1-methyl-2-nitrobenzene 
• 201486-48-8 N-[2-(2,2-Dimethoxy-ethyl)-phenyl]-4-(4-methoxy-phenoxy)-butyramide 
• 1969-73-9 (2-nitrophenyl)acetaldehyde 
• 201486-52-4 1-Indol-1-yl-4-(4-methoxy-phenoxy)-butan-1-one 
• 79844-33-0 2-(2-nitrophenyl)acetaldehyde dimethyl acetal 
• 150760-45-5 2-(2,2-dimethoxyethyl)-benzeneamine 
• 119-66-4 2-nitrobenzenediazonium chloride 
• 20973-67-5 N,N-dimethyl-2-(2-nitrophenyl)ethenylamine 
• 7318-34-5 1-(2-nitrophenyl)-4-chloro-2-butene 

Downstream Products

• 201486-63-7 4-(4-methoxyphenoxyl)butyraldehyde 

Relevant articles and documents

2-(2-aminophenyl)-acetaldehyde dimethyl acetal: A novel reagent for the protection of carboxylic acids

The synthesis and use of 2-(2-aminophenyl)-acetaldehyde dimethyl acetal 1 are described. The amides 2, derived from this amine and carboxylic acids, are stable under basic conditions and thus can be regarded as the protected carboxylic acids. The corresponding carboxylic acids are regenerated by conversion of 2 into indolylamides 3 by treatment with CSA and subsequent hydrolysis with LiOOH or NaOH. In addition, 3 can be easily converted to esters, amides, and aldehydes.