3911-49-7

Basic information

• Product Name: (4-nitrophenyl)(diphenyl)methanol
• Synonyms: (4-Nitrophenyl)(diphenyl)methanol; benzenemethanol, 4-nitro-alpha,alpha-diphenyl-
• CAS NO: 3911-49-7
• Molecular Formula: C₁₉H₁₅NO₃
• Molecular Weight: 305.3273
• Mol File: 3911-49-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 490.3°C at 760 mmHg
• Flash Point: 200°C
• Density: 1.261g/cm³
• Vapor Pressure: 1.99E-10mmHg at 25°C
• Refractive Index: 1.643
• CAS DataBase Reference: (4-nitrophenyl)(diphenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-nitrophenyl)(diphenyl)methanol(3911-49-7)
• EPA Substance Registry System: (4-nitrophenyl)(diphenyl)methanol(3911-49-7)

Safety Data

• Hazardous Substances Data: 3911-49-7(Hazardous Substances Data)

Usage

Description

(4-nitrophenyl)(diphenyl)methanol is a benzyl alcohol derivative with the molecular formula C19H15NO3. It features a nitrophenyl group and two phenyl groups attached to a central methanol backbone, making it a versatile compound in various fields.

Uses

Used in Organic Synthesis:
(4-nitrophenyl)(diphenyl)methanol is used as a building block for the preparation of various pharmaceutical and agrochemical compounds due to its unique structure and functional groups.
Used in Materials Science:
(4-nitrophenyl)(diphenyl)methanol is used as a component in the development of new materials, taking advantage of its chemical properties and potential interactions with other molecules.
Used as a Ligand in Coordination Chemistry:
(4-nitrophenyl)(diphenyl)methanol is used as a ligand to form coordination complexes with metal ions, which can have applications in catalysis, sensing, and other areas.
Used in Antimicrobial Agents Development:
(4-nitrophenyl)(diphenyl)methanol is used as a potential active ingredient in the development of new antimicrobial agents, given its demonstrated antibacterial and antifungal properties.

Upstream product

• 2945-12-2 1-(diphenylmethyl)-4-nitrobenzene 
• 74087-85-7 3,3-dimethyldioxirane 
• 555-16-8 4-nitrobenzaldehdye 
• 71-43-2 benzene 
• 62516-66-9 ((4-nitrophenoxy)methylene)dibenzene 
• 865-47-4 potassium tert-butylate 
• 75-65-0 tert-butyl alcohol 
• 41273-47-6 4-nitro-trityl chloride 
• 63068-97-3 dichloro-(4-nitro-phenyl)-phenyl-methane 

Downstream Products

• 857587-05-4 bis-[4-(α-chloro-benzhydryl)-phenyl]-diazene 
• 128527-12-8 bis-[4-(α-hydroxy-benzhydryl)-phenyl]-diazene 
• 42365-21-9 bis-[4-(α-dehydro-benzhydryl)-phenyl]-diazene 
• 128527-13-9 bis-[4-(α-hydroxy-benzhydryl)-phenyl]-diazene-N-oxide 
• 858784-45-9 N,N'-bis-[4-(α-hydroxy-benzhydryl)-phenyl]-hydrazine 
• 13189-74-7 4-nitro-trityl azide 
• 95437-74-4 tert-butyl-(4-nitro-trityl)-peroxide 

Relevant articles and documents

A three-aryl alcohol compound and its synthesis method

The invention discloses a three-aryl alcohol compound and its synthetic method, relates to the field of organic synthesis. The method is in the aerobic environment in a non-protic solvent, such as the formula (I) will be a compound represented by the gene

Electron Apportionment in Cleavage of Radical Anions. 1. Nitro-Substituted Benzyl Phenyl Ethers

The radical anions of 4-nitrobenzyl phenyl ethers undergo cleavage at least 10E4 times faster than the radical anions of corresponding 4-nitrophenyl benzyl ethers despite a perceived thermodynamic advantage for the latter set of reactions.It is suggested that this results reflects a kinetic advantage for cleavage reactions which take place with regioconservation of spin density.