35478-71-8

Basic information

• Product Name: 2-diethylaminophenol
• Synonyms: 2-diethylaminophenol
• CAS NO: 35478-71-8
• Molecular Formula: C₁₀H₁₅NO
• Molecular Weight: 165.2322
• EINECS: 252-586-4
• Mol File: 35478-71-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 219°C at 760 mmHg
• Flash Point: 86.3°C
• Appearance: /
• Density: 1.04g/cm³
• Vapor Pressure: 0.0828mmHg at 25°C
• Refractive Index: 1.564
• CAS DataBase Reference: 2-diethylaminophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-diethylaminophenol(35478-71-8)
• EPA Substance Registry System: 2-diethylaminophenol(35478-71-8)

Safety Data

• Hazardous Substances Data: 35478-71-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H15NO/c1-3-11(4-2)9-7-5-6-8-10(9)12/h5-8,12H,3-4H2,1-2H3

Upstream product

• 16790-23-1 N,N-Diethyl-2-ethoxyaniline 
• 91-66-7 N,N-diethylaniline 
• 826-42-6 N,N-diethylaniline N-oxide 
• 610-67-3 1-ethoxy-2-nitrobenzene 
• 94-70-2 ortho-phenitidine 

Downstream Products

• 103402-07-9 tetra-N-ethyl-2,2'-butanediyldioxy-di-aniline 
• 103401-46-3 tetra-N-ethyl-2,2'-pentanediyldioxy-di-aniline 
• 103510-09-4 tetra-N-ethyl-2,2'-hexanediyldioxy-di-aniline 
• 5809-23-4 2'-Carboxy-4-diethylamino-2-hydroxybenzophenon 
• 1330557-39-5 9'-diethylamino-3'-bromobenzo[a]fluoran 
• 1353572-99-2 9'-diethylamino-2'-bromobenzo[a]fluoran 
• 1353573-04-2 9'-diethylamino-3'-(3-hydroxyphenyl)benzo[a]fluoran 
• 26628-47-7 9-(diethylamino)-3'H-spiro[benzo[a]xanthene-12,1'-isobenzofuran]-3'-one 
• 1353573-05-3 9'-diethylamino-3'-phenylbenzo[a]fluoran 
• 1353573-07-5 9'-diethylamino-2'-(3-hydroxyphenyl)benzo[a]fluoran 

Relevant articles and documents

Hydroxylation directe d'anilines en aminophenols

Anilines react with hydrogen peroxide in SbF5-HF to give aminophenols.The formation of the products can be accounted for by the reaction of the electrophile H3O2+ on the anilinium ions.For compounds 1a-4a, the reaction yields three possible aminophenols, the meta isomer being the major product.The process is more selective with ortho toluidine 5a and para toluidine 6a, giving aminophenol(s) 5c (42percent)) and 5e (21percent), and 6c (71percent), respectively.With meta toluidine 7a, only aminophenol 7d (35percent) can be isolated from the complex reaction mixture, ring substitution pattern of the substrate favoring para hydroxylation.