60854-00-4

Usage

Uses

Used in Pharmaceutical Industry:
2-NITRO-5-PHENOXY-PHENYLAMINE serves as a crucial intermediate in the synthesis of pharmaceuticals. Its chemical properties make it a valuable component in the development of new drugs and medicinal compounds, contributing to the advancement of treatments and therapies.
Used in Dye Industry:
In the dye industry, 2-NITRO-5-PHENOXY-PHENYLAMINE is utilized as an intermediate for the production of various dyes. Its chemical structure allows for the creation of a range of colors and hues, enhancing the dye manufacturing process.
Used in Organic Compounds Synthesis:
Beyond its applications in pharmaceuticals and dyes, 2-NITRO-5-PHENOXY-PHENYLAMINE is also employed as an intermediate in the synthesis of other organic compounds. Its versatility in chemical reactions facilitates the creation of a diverse array of organic products.
Safety Precautions:
Given its classification as a mutagen, 2-NITRO-5-PHENOXY-PHENYLAMINE may pose a risk to human health if not managed properly. Therefore, it is imperative to adhere to stringent safety protocols when handling and using 2-NITRO-5-PHENOXY-PHENYLAMINE. This includes the use of appropriate personal protective equipment, ensuring proper ventilation, and following guidelines for safe storage and disposal.

Upstream product

• 620-88-2 4-nitrophenyl phenyl ether 
• 7664-93-9 sulfuric acid 
• 60853-99-8 N-(2-nitro-4-phenoxyphenyl)acetamide 
• 139-59-3 4-phenoxyanilin 
• 6312-87-4 p-phenoxyacetanilide 

Downstream Products

• 855761-40-9 8-nitro-6-phenoxy-quinoline 
• 58306-59-5 2-propionamido-5-phenoxyaniline 
• 1120345-76-7 7-nitro-5-phenoxy-1H-indole-2-carboxylic acid methyl ester 
• 1120334-11-3 2-bromo-6-nitro-4-phenoxyphenylamine 
• 59011-08-4 C₁₉H₂₁N₃O₄S 
• 854259-28-2 (4-bromo-phenyl)-(3,4-dichloro-phenyl)-ether 
• 854258-44-9 (4-chloro-3-iodo-phenyl)-phenyl ether 
• 854259-78-2 (3-bromo-4-chloro-phenyl)-phenyl ether 
• 55538-69-7 1,2-dichloro-4-phenoxybenzene 
• 860584-82-3 5-phenoxy-2-iodoaniline 
• 74865-98-8 2-chloro-5-phenoxyaniline 
• 63646-51-5 3,4,4'-Trichlorobiphenyl ether 
• 10265-98-2 (4-chloro-3-nitro-phenyl)-phenyl ether 
• 857825-63-9 (4-iodo-3-nitro-phenyl)-phenyl ether 

Relevant academic research and scientific papers

Indole and indazole compounds as an inhibitor of cellular necrosis

The present invention refers to a formula (1) compounds of, pharmaceutically acceptable salts or isomers thereof thereof, and characterized by by containing as active ingredients-associated diseases, cell death and method for the prevention or treatment of relates and compositions. [Formula 1] In formula said R 1, R 2, R 3, R 4, R 5, R 6, A, X, n and m to equal the specification.

INDOLE AND INDAZOLE COMPOUNDS AS AN INHIBITOR OF CELLULAR NECROSIS

The present invention relates to indole or indazole compounds, pharmaceutically acceptable salts or isomers thereof which are useful for the prevention or treatment of cellular necrosis and necrosis-associated diseases. The present invention also relates to a method and a composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases, comprising said indole or indazole compounds as an active ingredient.

INDOLE COMPOUNDS AS AN INHIBITOR OF CELLULAR NECROSIS

The present invention relates to new indole compounds, pharmaceutically acceptable salts or isomers thereof which are useful for the prevention or treatment of cellular necrosis and necrosis-associated diseases. The present invention also relates to a method and a composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases, comprising said indole compounds as an active ingredient.

INDOLE AND INDAZOLE COMPOUNDS AS AN INHIBITOR OF CELLULAR NECROSIS

The present invention relates to indole or indazole compounds, pharmaceutically acceptable salts or isomers thereof which are useful for the prevention or treatment of cellular necrosis and necrosis-associated diseases. The present invention also relates to a method and a composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases, comprising said indole or indazole compounds as an active ingredient.

INDOLE COMPOUNDS AS AN INHIBITOR OF CELLULAR NECROSIS

The present invention relates to new indole compounds, pharmaceutically acceptable salts or isomers thereof which are useful for the prevention or treatment of cellular necrosis and necrosis-associated diseases. The present invention also relates to a method and a composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases, comprising said indole compounds as an active ingredient.

Substituted (alkoxycarbonylthioureido)-(acylamino)-benzene derivatives

Benzene derivatives of the formula: STR1 wherein R1 represents alkyl, R2 represents a group --SR3, --SOR3, --SO2 R3, --OR3, --SCONH2, --SCN or --T(CH2)m T1 R4 [wherein R3 represeents alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, unsubstituted or substituted aryl, or cycloalkylalkyl, R4 represents hydrogen or alkyl, T and T1 each represent oxygen, sulphur or sulphinyl, and m is an integer from 1 to 7] whose position on the benzene ring is either para to the group --NHCSNHCOOR1 or para to the group --NHCOAZ, A represents a bivalent straight-chain aliphatic hydrocarbon radical of 1 to 4 carbon atoms or a said hydrocarbon radical substituted by at least one methyl group, and Z represents a group of the formula:- STR2 wherein R5 represents hydrogen or alkyl, R6 represents hydrogen, alkyl or phenylalkyl, and R7 represents hydrogen or alkyl, or R6 and R7 together with the nitrogen atom to which they are attached form a 5-,6- or 7-membered heterocyclic ring optionally substituted by alkyl group(s), and X- represents a pharmaceutically acceptable anion, are new compounds useful as anthelmintics and antifungal agents.

5(6)-Benzene ring substituted benzimidazole-2-carbamate derivatives having anthelmintic activity

Benzene ring substituted benzimidazole-2-carbamate derivatives represented by the formula: SPC1 Where R is a lower alkyl group having 1 to 4 carbon atoms; R1 is --SR5 or --OR5 ; and R5 is aryl. The R1 substitution is at the 5(6)-position. The compounds are useful as pesticides, particularly as anthelmintic and antifungal agents.