96898-75-8

Usage

Uses

Used in Pharmaceutical Industry:
4-CHLORO-3-NITROBENZAMIDE OXIME is used as an intermediate in the production of pharmaceuticals for its ability to facilitate the synthesis of various medicinal compounds.
Used in Organic Synthesis:
4-CHLORO-3-NITROBENZAMIDE OXIME is employed as a reagent in organic synthesis, playing a crucial role in the formation of a range of organic compounds.
Used in Chemical Research:
4-CHLORO-3-NITROBENZAMIDE OXIME is used as a building block in the creation of more complex chemicals, contributing to the advancement of chemical research and development.
Safety Precautions:
It is essential to handle 4-CHLORO-3-NITROBENZAMIDE OXIME with care due to its harmful nature if swallowed or inhaled, and its potential to cause skin and eye irritation. Adherence to proper safety precautions and handling procedures is imperative when working with this chemical.

Upstream product

• 939-80-0 4-chloro-3-nitrobenzonitrile 

Downstream Products

• 96898-95-2 3-(4-chloro-3-nitrophenyl)-1,2,4-oxadiazole 
• 862298-33-7 N'-acetyloxy-4-chloro-3-nitrobenzenecarboximideamide 
• 862298-34-8 4-chloro-N'-[(cyclopropylcarbonyl)oxy]-3-nitrobenzenecarboximideamide 
• 187399-90-2 5-(Chloromethyl)-3-(4'-chloro-3'-nitrophenyl)-1,2,4-oxadiazole 

Relevant academic research and scientific papers

((11-OXO-10,11-DIHYDRODIBENZO [B, F] [1, 4] OXAZEPIN-1-YL)OXY) ACETIC ACID DERIVATIVES AND RELATED COMPOUNDS AS CARDIOVASCULAR PREPARATIONS USED TO TREAT ARTERIOLOSCLEROSIS

The invention relates to dibenzoxazepines and to a method for the production thereof, use thereof in the treatment and/or prophylaxis of illnesses, in addition to the use thereof in the production of medicaments for treating and/or for the prophylaxis of diseases, in particular cardiovascular illnesses, e.g. arteriolosclerosis, and cancers: Said dibenzoxazepines are represented by formula (I), wherein R2 represents C1-C6-alkyl, alkyl can be substituted by 1 or 2 substituents, said substituents are selected independently from each other from the group consisting of halogen, hydroxy, oxo, C1-C6-alkoxy, hydroxycarbonyl, C1-C6-alkoxycarbonyl, aminocarbonyl and C1-C6-alkylaminocarbonyl, R3 represents O-CH2CO2H or -O-(CH2)2CO2H, R5 represents 5- 10-membered heteroaryl, -SO2-R6 or -NR7(C=O)R8, whereby heteroaryl can be substituted by 1, 2 or 3 substituents, said substituents being selected independently from each other from the group consisting of halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro, amino, C1-C6 alkylamino, hydroxy, C1-C6-alkyl, C1-C6-aIkoxy, hydroxycarbonyl, C1-C6-alkoxycarbonyl, amino-carbonyl, C1-C6-alkylaminocarbonyl, C6-C10-aryl and C3-C8-aycloalkyl. The other substituents are defined in the claims.