87671-67-8

Basic information

• Product Name: 2-[(4-methylphenyl)amino]phenol
• Synonyms: 2-[(4-methylphenyl)amino]phenol
• CAS NO: 87671-67-8
• Molecular Weight: 199.252
• Mol File: 87671-67-8.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2-[(4-methylphenyl)amino]phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-methylphenyl)amino]phenol(87671-67-8)
• EPA Substance Registry System: 2-[(4-methylphenyl)amino]phenol(87671-67-8)

Safety Data

• Hazardous Substances Data: 87671-67-8(Hazardous Substances Data)

Upstream product

• 133437-35-1 2-benzylamino-4'-methyldiphenyl ether 
• 273-53-0 benzoxazole 
• 624-31-7 4-tolyl iodide 
• 928642-45-9 6-diazo-2-cyclohexen-1-one 
• 106-49-0 p-toluidine 
• 585526-04-1 N-(4-methoxy-4-methylcyclohexa-2,5-dien-1-ylidene)-4-methylbenzenesulfonamide 
• 599-86-0 4-methyl-N-(4-methylphenyl)benzenesulfonamide 
• 64-19-7 acetic acid 
• 95-55-6 2-amino-phenol 
• 106-38-7 para-bromotoluene 
• 20927-98-4 2-p-tolyloxy-aniline 
• 58656-56-7 2,3-dihydro-2,2-dimethoxy-2-phenyl-3-p-tolyl-1,3,2-benzoxazaphosph(V)ole 
• 87671-57-6 2,2-diethoxy-2,3-dihydro-2-phenyl-3-p-tolyl-1,3,2-benzoxazaphosph(V)ole 
• 133437-34-0 2-allylamino-4'-methyldiphenyl ether 

Downstream Products

• 107455-62-9 N-(2-methoxyphenyl)-4-methylaniline 

Relevant articles and documents

COMPOUND WHICH INHIBITS TELOMERE-BINDING PROTEIN, AND TELOMERE-BINDING PROTEIN INHIBITOR CONTAINING SAME

The compound according to the present invention is a compound represented by the following chemical formula: wherein, in the above-described chemical formula, R1 is oxygen or sulfur, and R2 to R6 are each independently sel

A method of synthesis of natural product Glycozolicine

The invention discloses a method for synthesizing a natural product Glycozolicine, and belongs to the field of organic synthesis. The method comprises the following steps: catalyzing the reaction of 6-diazo-2-cyclohexene-1-ketone and paratoluidine by usin

One-pot synthesis of diarylamines from two aromatic amines via oxidative dearomatization-imino exchange-reductive aromatization

A one-pot synthetic strategy for diarylamines using only aromatic amines as starting materials has been developed. This method involved a PhI(OAc) 2-induced oxidative dearomatization of N-sulfonyl protected para-substituted anilines, a Bi(OTf)3-catalyzed imino exchange reaction between N-sulfonyl cyclohexadienimines and aromatic amines, and a CF3COOH/Zn mediated reductive aromatization of the resulting N-aryl cyclohexadienimines.