52744-72-6

Basic information

• Product Name: (2-aminophenyl)diphenylmethanol
• Synonyms: (2-aminophenyl)diphenylmethanol
• CAS NO: 52744-72-6
• Molecular Weight: 275.35
• Mol File: 52744-72-6.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: (2-aminophenyl)diphenylmethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-aminophenyl)diphenylmethanol(52744-72-6)
• EPA Substance Registry System: (2-aminophenyl)diphenylmethanol(52744-72-6)

Safety Data

• Hazardous Substances Data: 52744-72-6(Hazardous Substances Data)

Usage

Description

(2-aminophenyl)diphenylmethanol is a chemical compound with the molecular formula C19H17NO. It is a white to off-white solid that is slightly soluble in water and has a molecular weight of 279.34 g/mol. (2-aminophenyl)diphenylmethanol is used in the synthesis of various pharmaceutical compounds and has applications in the field of organic chemistry. It has been studied for its potential as a building block for the synthesis of biologically active molecules. Additionally, (2-aminophenyl)diphenylmethanol has been investigated for its potential use in the development of new materials with specific properties, such as fluorescence and luminescence. Overall, this compound has diverse potential applications and is of interest to researchers in various scientific fields.

Uses

Used in Pharmaceutical Synthesis:
(2-aminophenyl)diphenylmethanol is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
(2-aminophenyl)diphenylmethanol is used as a reagent and intermediate in various organic chemical reactions. Its versatility and stability contribute to its utility in the synthesis of complex organic molecules.
Used in Material Science:
(2-aminophenyl)diphenylmethanol is used as a precursor in the development of new materials with specific properties, such as fluorescence and luminescence. Its potential applications in this field include the creation of advanced sensors, imaging agents, and optoelectronic devices.
Used in Research and Development:
(2-aminophenyl)diphenylmethanol is used as a research compound in various scientific fields, including chemistry, biology, and materials science. Its diverse potential applications make it an interesting subject for further study and exploration.

Upstream product

• 71526-47-1 4,4-diphenyl-1,4-dihydro-3,1-benzoxazin-2(1H)-one 
• 82757-19-5 2-formamidotriphenylmethanol 
• 16714-27-5 (2-azidophenyl)(phenyl)methanone 
• 100-58-3 phenylmagnesium bromide 
• 108-86-1 bromobenzene 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 100-59-4 phenylmagnesium chloride 
• 87-25-2 2-ethoxycarbonylaniline 
• 134-20-3 2-carbomethoxyaniline 
• 71-43-2 benzene 
• 5100-23-2 2-isocyanatobenzoyl chloride 
• 10113-38-9 N-(2-bromophenyl)formamide 
• 119-61-9 benzophenone 
• 101894-63-7 (2-amino-3,5-dibromo-phenyl)-diphenyl-methanol 

Downstream Products

• 67695-84-5 α-(2-Benzamidophenyl)benzohydrol 
• 50547-57-4 2-ethyl-4,4-diphenyl-4H-benzo[d][1,3]oxazine 
• 120759-23-1 2-(5-bromo-2-furyl)-4,4-diphenyl-1,2-dihydro-4H-3,1-benzoxazine 
• 120759-22-0 2-[2-(5-Methyl-furan-2-yl)-ethyl]-4,4-diphenyl-1,4-dihydro-2H-benzo[d][1,3]oxazine 
• 681850-07-7 C₂₆H₁₉BrN₂O₄ 
• 382174-92-7 2-(2-hydroxyphenyl)-4,4-diphenyl-1,4-dihydro-2H-1,3-benzoxazine 
• 312527-47-2 2-(2-hydroxy-5-nitrophenyl)-4,4-diphenyl-1,4-dihydro-2H-1,3-benzoxazine 
• 443332-63-6 C₂₆H₂₀BrNO₂ 
• 872786-15-7 1,1,2-triphenyl-1H-indene 

Relevant articles and documents

Organocatalytic Atroposelective Construction of Axially Chiral N-Aryl Benzimidazoles Involving Carbon-Carbon Bond Cleavage

Axially chiral compounds widely occur in natural products, biologically active molecules, ligands, and catalysts, and their efficient and enantioselective synthesis is highly desirable. Herein, we report a novel method for the atroposelective construction of axially chiral N-aryl benzimidazoles with chiral phosphoric acid as the organocatalyst via reaction of N1-(aryl)benzene-1,2-diamines with multicarbonyl compounds. The present method provided the target products in high yields (up to 89percent) with excellent enantioselectivity (up to 98percent ee).

Carbon isotope labeling of carbamates by late-stage [11C], [13C] and [14C]carbon dioxide incorporation

A general procedure for the late-stage [11C], [13C] and [14C]carbon isotope labeling of cyclic carbamates is reported. This protocol allows the incorporation of carbon dioxide, the primary source of carbon-14 and carbon-11 radioisotopes, in a direct, cost-effective and sustainable manner. A disconnection/reconnection strategy, involving ring opening/isotopic closure, was also implemented.

Copper-Catalyzed One-Pot Synthesis of Dibenzofurans, Xanthenes, and Xanthones from Cyclic Diphenyl Iodoniums

Oxygenation of cyclic diphenyl iodoniums (CDPIs) with varied medium-ring sizes has been fully investigated. This practical copper-catalyzed tandem reaction of CDPIs with water as the oxygen source enables the construction of derivatised dibenzofurans and xanthenes at moderate to good yields. Moreover, structurally important xanthones are also successfully accessed under the oxygenation conditions with additional TEMPO.