5461-78-9

Usage

General Description

The chemical 2-[(2-hydroxy-5-nitro-phenyl)methyl]-4-nitro-phenol, also known as Lasalocid, is a compound with a molecular formula C19H19N3O8. It is commonly used as an antibiotic and coccidiostat in veterinary medicine, particularly for the control of coccidiosis in poultry, cattle, and other animals. It works by disrupting the ion transport in the cell membranes of the coccidia parasites, leading to their death. Lasalocid is also used as a growth promoter in some animal feeds to improve feed efficiency and animal growth. However,

Upstream product

• 50-00-0 formaldehyd 
• 100-02-7 4-nitro-phenol 
• 7664-93-9 sulfuric acid 

Downstream Products

• 39612-32-3 4,6,4',6'-tetranitro-2,2'-methanediyl-di-phenol 
• 105245-83-8 2,2'-methylenebis(4-nitrophenylacetate) 
• 105245-85-0 15,21-dinitro-2,5,8,11-tetraoxatricyclo<17,4,0,0^12,17>tricosa-1(23),12,14,16,19,21-hexaene 
• 227001-45-8 2-(2-propoxy-5-nitrobenzyl)-4-nitrophenyl propyl ether 
• 27206-57-1 2,2'-methylene-bis(4-nitromethoxybenzene) 
• 1272641-38-9 2,2'-methylenebis(1-dodecyloxy-4-nitrobenzene) 
• 114164-34-0 bis-(2-ethoxy-5-ureido-phenyl)-methane 
• 3921-33-3 4,4'-diethoxy-3,3'-methanediyl-di-aniline 
• 227001-47-0 6,6'-bis-(2-propoxy-5-nitrobenzyl)-4,4'-dinitro-2,2'-methanediyl-di(phenyl propyl ether) 
• 227001-51-6 6,6'-bis-(2-propoxy-5-aminobenzyl)-4,4'-diamino-2,2'-methanediyl-di(phenyl propyl ether) 
• 227001-49-2 2-(2-propoxy-5-aminobenzyl)-4-aminophenyl propyl ether 
• 59920-13-7 6,6'-bis-(2-hydroxy-5-nitrobenzyl)-4,4'-dinitro-2,2'-methanediyl-diphenol 
• 178818-88-7 2-(2-octadecyloxy-5-nitrobenzyl)-4-nitrophenyl octadecyl ether 
• 130728-50-6 bis-(2-ethoxy-5-nitro-phenyl)-methane 

Relevant academic research and scientific papers

Synthesis, characterization, and catalytic activity of a new series of Ni(II), Cu(II), and Zn(II) complexes of N,N-O,O mixed-bidentate ligands for C–C cross-coupling reactions

A new series of air stable transition metal(II) complexes [M(II)(L)(Phen)], [M(II)(L)(Pip)] (M = Ni, Cu, and Zn) (H2L = 2,2′-methylenebis(4-nitrophenol)) (Phen =1,10-phenanthroline) (Pip = Piperazine) has been synthesized by incorporating the metal ion with bisphenol and 1,10-phenanthroline/piperazine ligands. The prepared metal complexes were characterized by FT-IR, UV–vis, 1H NMR, EPR, and mass spectrometry. The metal(II) complexes were potent catalysts for Suzuki–Miyaura and Kumada–Corriu coupling of various aryl halides under optimized conditions.

Hirshfeld surface analysis of substituted phenols

The effect of para-substituents on the crystal packing of phenols has been investigated, for systems bearing nonpolar groups (tert-butyl and benzyl, compounds 1 and 2, respectively) and for methylene linked bis-phenol bearing polar nitro groups (compound

Supramolecular layers and versatile packing modes: The solid state behavior of ortho, ortho-linked bisphenols

A series of ortho-ortho-linked bisphenols featuring electron-withdrawing groups (EWGs) attached to the phenolic rings is reported. Their respective molecular structures and packing behaviors have been studied by X-ray diffraction, comparatively discussed

PHOTO-RESPONSIVE LIQUID CRYSTALLINE COMPOUND AND ITS APPLICATIONS

The purpose of the present invention is to provide novel liquid crystalline compounds that are capable of inducing phase transition by a light stimulus and are useful in the display, optoelectronics, and photonics field. The present invention relates to t

Synthesis and characterization of new crown ethers of Schiff base type and their complexes

New crown ether ligands of Schiff base type (4-11) have been synthesised by the reaction of two equivalents of benzaldehyde, 2-hydroxybenzaldehyde, 2,3-dihydroxybenzaldehyde, 5-methoxy-2-hydroxybenzaldehyde, 5-bromo-2- hydroxybenzaldehyde, 5-nitro-2-hydro

Calixarenes with diphenylphosphoryl acetamide functions at the upper rim. A new class of highly efficient extractants for lanthanides and actinides

Various calix[4]arene tetraalkyl ethers and a calix[5]arene pentaalkyl ether substituted at the upper rim by the CMPO-like functional group -NH-C(O)-CH2-P(O)Ph2 as well as some linear model compounds have been synthesized for the fir

THE SYNTHESIS OF ASYMMETRIC MACROCYCLIC POLYETHERS CONTAINING NITRO GROUP ON AROMATIC RING

The macrocyclic polyether : 12,18-dinitro-2,5,8-trioxatricyclo(14,4,0,09,14)eicosa-1(20),9,11,13,16,18 hexaene (6): 15,21-dinitro-2,5,8,11-tetraoxatricyclo(17,4,0,012,17)tricosa-1(23),12,14,16,19,21-hexaene (7) and 18,24-dinitro-2,5,8,11,14-pentaoxatricyclo)20,4,0,015,20)hexacosa-1(26),15,17,19,22,24-hexaene (8) have been synthesized by reaction of 2,2'-methylenebis(4-nitrophenol) (1) with diethylene glycol ditosylate (3) triethylene glycol ditosylate (4) and tetraethylene glycol ditosylate (5) respectively in the presence of KOBu-t.These compounds did not form stable complexes with alkali and alkaline-earth cations.The macrocyclic polyethers were purified by chromatoraphy and crystallization.The structure of these new compounds have been determined by elemental analysis, molecular weight determination, 1H NMR, IR and UV spectra.