13086-92-5

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

• 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 
• 29367-40-6 2-(3-tert-Butyl-4-hydroxy-5-methyl-benzyl)-2-(3,5-di-tert-butyl-4-hydroxy-benzyl)-malonic acid dioctadecyl ester 

Relevant academic research and scientific papers

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

Method of treating inflammatory bowel disease

Provided is a method for treating inflammatory bowel disease in mammals utilizing certain phenol and benzamide compounds.

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

Method of treating type I diabetes

Provided is a method for treating Type I diabetes in mammals utilizing certain phenol and benzamide compounds.

Chemical process for preparing 1,3 diketones

Novel (3',5'-dihydrocarbyl-4'-hydroxybenzyl)-1,3-diketones are prepared by reacting an N,N-dihydrocarbyl-2,6-dihydrocarbyl-4-aminomethylphenol with a 1,3-diketone in the presence of a basic substance. The products are useful as antioxidants.

Chemical process for preparing 1,3-diketones

Novel (3',5'-dihydrocarbyl-4'-hydroxybenzyl)-1,3-diketones are prepared by reacting an N,N-dihydrocarbyl-2,6-dihydrocarbyl-4-aminomethylphenol with a 1,3-diketone and an alkyl halide in the presence of an alkali or an alkaline earth metal hydride. The products are useful as antioxidants.

Chemical process

Novel 2,4-dihydrocarbylspiro[5.5]undeca-1,4,8-trien-3-one compounds are prepared by reacting an N,N-dihydrocarbyl,2,6-dihydrocarbyl-4-aminomethylphenol with a conjugated diene and an alkyl halide in a liquid solvent medium.