13086-92-5

Basic information

• Product Name: 4-(dimethylaminomethyl)-2-methyl-6-tert-butyl-phenol
• Synonyms: 4-(dimethylaminomethyl)-2-methyl-6-tert-butyl-phenol
• CAS NO: 13086-92-5
• Molecular Formula: C₁₄H₂₃NO
• Molecular Weight: 221.34
• Mol File: 13086-92-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 281.2°C at 760 mmHg
• Flash Point: 95.8°C
• Appearance: /
• Density: 0.973g/cm³
• Vapor Pressure: 0.00212mmHg at 25°C
• Refractive Index: 1.521
• CAS DataBase Reference: 4-(dimethylaminomethyl)-2-methyl-6-tert-butyl-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(dimethylaminomethyl)-2-methyl-6-tert-butyl-phenol(13086-92-5)
• EPA Substance Registry System: 4-(dimethylaminomethyl)-2-methyl-6-tert-butyl-phenol(13086-92-5)

Safety Data

• Hazardous Substances Data: 13086-92-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H23NO/c1-10-7-11(9-15(5)6)8-12(13(10)16)14(2,3)4/h7-8,16H,9H2,1-6H3

Upstream product

• 50-00-0 formaldehyd 
• 2219-82-1 2-tert-Butyl-6-methylphenol 
• 124-40-3 dimethyl amine 

Downstream Products

• 59735-09-0 2,2-Bis-(3-tert-butyl-4-hydroxy-5-methyl-benzyl)-malonic acid diethyl ester 
• 20297-75-0 2,2-Bis-(3-tert-butyl-4-hydroxy-5-methyl-benzyl)-malonic acid dibutyl ester 
• 20297-76-1 2,2-Bis-(3-tert-butyl-4-hydroxy-5-methyl-benzyl)-malonic acid dihexyl ester 
• 20297-77-2 2,2-Bis-(3-tert-butyl-4-hydroxy-5-methyl-benzyl)-malonic acid dioctyl ester 
• 59735-11-4 2-(3-tert-Butyl-4-hydroxy-5-methyl-benzyl)-3-(3-tert-butyl-4-hydroxy-5-methyl-phenyl)-2-cyano-propionic acid octadecyl ester 
• 59735-29-4 2,2-Bis-(3-tert-butyl-4-hydroxy-5-methyl-benzyl)-malonic acid bis-(2-butoxy-ethyl) ester 
• 59754-89-1 2-(3-tert-Butyl-4-hydroxy-5-methyl-benzyl)-2-(4-hydroxy-3,5-dimethyl-benzyl)-malonic acid dioctadecyl ester 
• 20370-19-8 2,2-Bis-(3-tert-butyl-4-hydroxy-5-methyl-benzyl)-malonic acid dioctadecyl ester 
• 59735-10-3 2-(3-tert-Butyl-4-hydroxy-5-methyl-benzyl)-3-(3-tert-butyl-4-hydroxy-5-methyl-phenyl)-2-cyano-propionic acid dodecyl ester 
• 59735-26-1 2,2-Bis-(3-tert-butyl-4-hydroxy-5-methyl-benzyl)-malonic acid bis-(3-methylsulfanyl-propyl) ester 
• 59735-25-0 2-(3-tert-Butyl-4-hydroxy-5-methyl-benzyl)-3-(3-tert-butyl-4-hydroxy-5-methyl-phenyl)-2-cyano-propionic acid 2-dodecylsulfanyl-ethyl ester 
• 59735-28-3 2-(3-tert-Butyl-4-hydroxy-5-methyl-benzyl)-3-(3-tert-butyl-4-hydroxy-5-methyl-phenyl)-2-cyano-propionic acid 3-hexadecylsulfanyl-propyl ester 
• 59735-27-2 2,2-Bis-(3-tert-butyl-4-hydroxy-5-methyl-benzyl)-malonic acid bis-(3-hexylsulfanyl-propyl) ester 
• 59735-24-9 2,2-Bis-(3-tert-butyl-4-hydroxy-5-methyl-benzyl)-malonic acid bis-(2-octylsulfanyl-ethyl) ester 

Relevant articles and documents

Direct Synthesis of Spiroundeca-1,4,7-trienones from Phenols via a Quinone Methide Intermediate

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Synthesis and study of the antiradical activity of substituted hydroxybenzylamines and their hydrogen chloride salts

Different alkylated hydroxybenzylamines and their hydrogen chloride salts were synthesized. The rate constants of their reactions with peroxide radicals k1 and the stoichiometric factors of inhibition f were measured in the initiated oxidation of cumene and methyl oleate. Copyright

Heterocyclic Spirocyclohexadienones from Substituted Phenols

Mannich bases were prepared from substituted phenols with aliphatic amines and formaldehyde.Amine exchange with N-methyl-2-naphthylamine followed by a Hofmann Martius rearrangement gave rise to o,o'-amino-hydroxy-diphenylmethane derivatives.Under cyclization conditions some of these compounds produced spirocyclohexadienones, which are the ipso analogs to the hypothetic intermediates postulated in the aminomethylation mechanism of phenols. - Keywords: Mannich Reaction; Phenol Dienone Tautomerism; Hofmann Martius Rearrangement