13159-73-4 Usage
Description
N-(2-Hydroxybenzyl)-4-nitroaniline is a chemical compound characterized by a 4-nitroaniline moiety connected to a benzyl group, which features a hydroxyl substituent at the ortho position. This aromatic compound is recognized for its potential as a dye precursor and its utility in organic synthesis, research, and pharmaceutical development.
Uses
Used in Organic Synthesis:
N-(2-Hydroxybenzyl)-4-nitroaniline is used as a starting material in organic synthesis for the preparation of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of a wide range of products.
Used in Research:
In research settings, N-(2-Hydroxybenzyl)-4-nitroaniline serves as a key compound for studying chemical reactions and exploring new synthetic pathways. Its reactivity and structural features contribute to the advancement of chemical knowledge and the development of novel methodologies.
Used in Dye Industry:
Due to its aromatic nature and ability to participate in various chemical reactions, N-(2-Hydroxybenzyl)-4-nitroaniline is used as a dye precursor in the dye industry. Its potential to create a spectrum of colors makes it a promising candidate for the development of new dyes and pigments.
Used in Pharmaceutical Industry:
N-(2-Hydroxybenzyl)-4-nitroaniline has demonstrated potential applications in the pharmaceutical industry, particularly in the development of novel drugs and pharmaceutical products. Its chemical properties and reactivity make it a candidate for the creation of new therapeutic agents and formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 13159-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13159-73:
(7*1)+(6*3)+(5*1)+(4*5)+(3*9)+(2*7)+(1*3)=94
94 % 10 = 4
So 13159-73-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O3/c16-13-4-2-1-3-10(13)9-14-11-5-7-12(8-6-11)15(17)18/h1-8,14,16H,9H2
13159-73-4Relevant articles and documents
A simple method for the reduction of Schiff bases using biosynthesized nickel oxide nanoparticles
Muthuvinothini, Alagesan,Stella, Selvaraj
, p. 267 - 271 (2021)
An innovative and simple approach for the reduction of aldimines to the corresponding secondary amines was described using biosynthesized nickel oxide nanoparticles as heterogeneous catalyst and ammonium formate as the hydrogen donor. This catalytic trans
Structure-activity relationship study of E6 as a novel necroptosis inducer
Mou, Jianfeng,Park, Ann,Cai, Yu,Yuan, Junying,Yuan, Chengye
supporting information, p. 3057 - 3061 (2015/06/22)
Necroptosis inducers represent a promising potential treatment for drug-resistant cancer. We herein describe the structure modification of E6, which was identified recently as a potent and selective necroptosis inducer. The studies described herein demonstrate for the first time that functionalized biphenyl derivatives possess necroptosis inducer activity. Furthermore, these studies have led to the identification of two promising compounds (5h and 5j) that can be used for further optimization studies as well as mechanism of action investigations.
Sodium borohydride on wet clay: Solvent-free reductive amination of carbonyl compounds using microwaves
Varma, Rajender S.,Dahiya, Rajender
, p. 6293 - 6298 (2007/10/03)
A solvent-flee reductive amination of carbonyl compounds by wet montmorillonite K 10 clay supported sodium borohydride is described; microwave irradiation facilitates the procedure.
