5461-78-9

Basic information

• Product Name: 2-[(2-hydroxy-5-nitro-phenyl)methyl]-4-nitro-phenol
• CAS NO: 5461-78-9
• Molecular Formula: C₁₃H₁₀N₂O₆
• Molecular Weight: 290.232
• Mol File: 5461-78-9.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 576.4°Cat760mmHg
• Flash Point: 244.3°C
• Density: 1.532g/cm³
• CAS DataBase Reference: 2-[(2-hydroxy-5-nitro-phenyl)methyl]-4-nitro-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2-hydroxy-5-nitro-phenyl)methyl]-4-nitro-phenol(5461-78-9)
• EPA Substance Registry System: 2-[(2-hydroxy-5-nitro-phenyl)methyl]-4-nitro-phenol(5461-78-9)

Safety Data

• Hazardous Substances Data: 5461-78-9(Hazardous Substances Data)

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

• 178818-88-7 2-(2-octadecyloxy-5-nitrobenzyl)-4-nitrophenyl octadecyl ether 
• 100865-19-8 C₁₅H₁₂Br₂N₂O₆ 
• 227001-45-8 2-(2-propoxy-5-nitrobenzyl)-4-nitrophenyl propyl ether 
• 1272641-38-9 2,2'-methylenebis(1-dodecyloxy-4-nitrobenzene) 
• 27206-57-1 2,2'-methylene-bis(4-nitromethoxybenzene) 
• 178818-89-8 2-(2-octadecyloxy-5-aminobenzyl)-4-aminophenyl octadecyl ether 
• 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 
• 130728-50-6 bis-(2-ethoxy-5-nitro-phenyl)-methane 
• 105245-83-8 2,2'-methylenebis(4-nitrophenylacetate) 
• 114164-34-0 bis-(2-ethoxy-5-ureido-phenyl)-methane 
• 3921-33-3 4,4'-diethoxy-3,3'-methanediyl-di-aniline 
• 39612-32-3 4,6,4',6'-tetranitro-2,2'-methanediyl-di-phenol 
• 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) 

Relevant articles and documents

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.

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

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