851233-24-4

Basic information

• Product Name: (4-(bis(4-(tert-butyl)phenyl)amino)phenyl)boronic acid
• Synonyms: (4-(bis(4-(tert-butyl)phenyl)amino)phenyl)boronic acid
• CAS NO: 851233-24-4
• Molecular Weight: 401.357
• Mol File: 851233-24-4.mol

Chemical Properties

• Boiling Point: 559.9±60.0 °C(Predicted)
• Density: 1.10±0.1 g/cm3(Predicted)
• CAS DataBase Reference: (4-(bis(4-(tert-butyl)phenyl)amino)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(bis(4-(tert-butyl)phenyl)amino)phenyl)boronic acid(851233-24-4)
• EPA Substance Registry System: (4-(bis(4-(tert-butyl)phenyl)amino)phenyl)boronic acid(851233-24-4)

Safety Data

• Hazardous Substances Data: 851233-24-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(4-(bis(4-(tert-butyl)phenyl)amino)phenyl)boronic acid is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure allows for the creation of new chemical entities and the modification of existing compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (4-(bis(4-(tert-butyl)phenyl)amino)phenyl)boronic acid is used as a building block for the development of new drugs. Its ability to form stable complexes with various molecules makes it a valuable component in the synthesis of potential therapeutic agents.
Used in Agrochemical Development:
Similarly, in the agrochemical industry, this boronic acid is utilized for the development of new agrochemicals. Its complex-forming properties enable the creation of novel compounds with potential applications in agriculture, such as pesticides and herbicides.
Used in Materials Science:
(4-(bis(4-(tert-butyl)phenyl)amino)phenyl)boronic acid is also used in the field of materials science. It is employed in the development of functional coatings and polymer materials, where its complex-forming ability contributes to the enhancement of material properties and performance.

Upstream product

• 137350-54-0 4-(1,1-dimethylethyl)-N-[4-(1,1-dimethylethyl)phenyl]-N-phenyl-benzenamine 
• 121-43-7 Trimethyl borate 
• 851233-23-3 N-(4-bromophenyl)-4-tert-butyl-N-(4-tert-butylphenyl)benzenamine 

Downstream Products

• 1415100-81-0 2,2-dimethyl-1,3-propanediol 4-bis(4-tert-butylphenylamino)phenylboronate 
• 1428876-42-9 C₆₁H₆₇N₃O₃S 

Relevant articles and documents

Self-assembled triphenylamine-hexaazatriphenylene two-photon absorption dyes

This paper reports the self-assembling and two-photon absorption natures of donor-acceptor molecules, tri(phenanthro)hexaazatriphenylene (TPHAT-C) and tri(phenanthrolino)hexaazatriphenylene (TPHAT-N), bearing six electron-donating moieties. In the 1H NMR spectra, a line-broadening effect, arising from self-assembled aggregation was observed. Several hundred nanometer scale aggregates were detected in dynamic light scattering. The one-dimensional aggregation of the TPHAT molecules was indicated by the concentration dependence in UV/vis one-photon absorption and one-photon excited fluorescence spectroscopies. An enhancement of the two-photon absorption cross-section was observed in the self-assembled TPHAT system. The order of the two-photon absorption nature is in agreement with the order of the aggregative nature.