30427-16-8

Basic information

• Product Name: 2-dimethylamino-p-cresol
• Synonyms: 2-dimethylamino-p-cresol;2-(Dimethylamino)-4-methylphenol
• CAS NO: 30427-16-8
• Molecular Formula: C₉H₁₃NO
• Molecular Weight: 151.20562
• EINECS: 250-192-7
• Mol File: 30427-16-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 218.7°Cat760mmHg
• Flash Point: 87.2°C
• Appearance: /
• Density: 1.063g/cm³
• Vapor Pressure: 0.0841mmHg at 25°C
• Refractive Index: 1.579
• CAS DataBase Reference: 2-dimethylamino-p-cresol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-dimethylamino-p-cresol(30427-16-8)
• EPA Substance Registry System: 2-dimethylamino-p-cresol(30427-16-8)

Safety Data

• Hazardous Substances Data: 30427-16-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H13NO/c1-7-4-5-9(11)8(6-7)10(2)3/h4-6,11H,1-3H3

Upstream product

• 121-72-2 N,N-dimethyl-m-toluidine 
• 825-80-9 m-methyl-N,N-dimethylaniline-N-oxide 
• 67-56-1 methanol 
• 2977-71-1 2-amino-4-methylphenol hydrochloride 

Downstream Products

• 80817-17-0 N-<1,1-(2)H2>allyl-2-hydroxy-5,NN-trimethylanilinium toluene-p-sulphonate 
• 79249-74-4 2-hydroxy-5,NN-trimethyl-N-(2-t-butylallyl)anilinium bromide 
• 79249-73-3 2-hydroxy-5,NN-trimethyl-N-(2-methylallyl)anilinium bromide 
• 80816-95-1 N-cinnamyl-2-hydroxy-5,NN-trimethylanilinium bromide 
• 79249-72-2 N-allyl-2-hydroxy-5,NN-trimethylanilinium bromide 
• 80817-11-4 2-cinnamyloxy-5,NN-trimethylaniline 
• 79249-81-3 N-(2-t-butylallyl)-5,NN-trimethylanilinium-2-olate 
• 79249-80-2 5,NN-trimethyl-N-(2-methylallyl)anilinium-2-olate 
• 79249-79-9 N-allyl-5,NN-trimethylanilinium-2-olate 

Relevant articles and documents

Metal-free functionalization of N, N-dialkylanilines via temporary oxidation to N, N-dialkylaniline N-oxides and group transfer

A simple set of protocols for the controlled elaboration of anilines is reported allowing access to a diverse array of aminophenols, aminoarylsulfonates, alkylated anilines, and aminoanilines in 29-95% yield in a single laboratory operation from easily isolable, bench-stable N,N-dialkylaniline N-oxides. The introduction of new C-O, C-C, and C-N bonds on the aromatic ring is made possible by a temporary increase in oxidation level and excision of a weak N-O bond.