22233-54-1

Usage

Uses

Used in Pharmaceutical Industry:
3-CHLORO-5-NITROBENZALDEHYDE is used as a key intermediate in the synthesis of various pharmaceuticals due to its versatile chemical structure and reactivity.
Used in Agrochemical Industry:
3-CHLORO-5-NITROBENZALDEHYDE is used as a precursor in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Dye Industry:
3-CHLORO-5-NITROBENZALDEHYDE is used as a dye intermediate for its strong yellow color, playing a crucial role in the formulation of various dyes and pigments.
Used in Organic Synthesis:
3-CHLORO-5-NITROBENZALDEHYDE is used as a reagent in organic synthesis for the preparation of other organic compounds, showcasing its utility in the synthesis of a wide range of chemical products.
Used in Antimicrobial and Antifungal Applications:
3-CHLORO-5-NITROBENZALDEHYDE is used in the development of new pharmaceuticals due to its antimicrobial and antifungal properties, offering potential in the creation of novel treatments for various infections.

InChI:InChI=1/C7H4ClNO3/c8-6-1-5(4-10)2-7(3-6)9(11)12/h1-4H

Upstream product

• 16582-38-0 3-chloro-5-nitrotoluene 
• 79944-62-0 (3-chloro-5-nitrophenyl)methanol 
• 90390-46-8 (3-amino-5-nitrophenyl)methanol 
• 71022-43-0 3,5-dinitrobenzyl alcohol 
• 23218-93-1 3-amino-5-nitro-benzoic acid methyl ester 
• 36138-28-0 3-chloro-5-nitro-benzoic acid methyl ester 

Downstream Products

• 67483-50-5 (E)-3-chloro-5,β-dinitro-styrene 
• 90390-38-8 (3-Chloro-5-nitro-benzyl)-methyl-amine 
• 90390-39-9 (3-Chloro-5-nitro-benzyl)-ethyl-amine 
• 90390-40-2 (3-Chloro-5-nitro-benzyl)-propyl-amine 
• 90390-41-3 Butyl-(3-chloro-5-nitro-benzyl)-amine 
• 960083-35-6 4-(3-chloro-5-nitro-phenyl)-1H-pyrrole-3-carbonitrile 
• 1615252-85-1 (S)-2,4-diamino-6-((1-(5-chloro-3-(3-chloro-5-(difluoromethyl)phenyl)-4-oxo-3,4-dihydroquinazolin-2-yl)ethyl)amino)pyrimidine-5-carbonitrile 
• 1615254-49-3 (S)-tert-butyl 1-(5-chloro-3-(3-chloro-5-(difluoromethyl)phenyl)-4-oxo-3,4-dihydroquinazolin-2-yl)ethylcarbamate 
• 1615256-04-6 (S)-2-(1-aminoethyl)-5-chloro-3-(3-chloro-5-(difluoromethyl)phenyl)quinazolin-4(3H)-one 
• 960083-34-5 3-(3-chloro-5-nitro-phenyl)-acrylonitrile 

Relevant academic research and scientific papers

PYRROLE DERIVATIVES WITH CRTH2 RECEPTOR MODULATOR ACTIVITY

There are provided according to the invention compounds of formula (I) in free or salt form, wherein R3, R 4, R5, R6a, R6b, Q and W are as described in the specification, process for preparing them, a

Synthesis and structure-activity relationships of 3-aminobenzophenones as antimitotic agents

A new series of 3-aminobenzophenone compounds as potent inhibitors of tubulin polymerization was discovered based on the mimic of the aminocombretastatin molecular skeleton. Lead compounds 5 and 11, with alkoxy groups at the C-4 position of B-ring, were p

Benzylamines: Synthesis and evaluation of antimycobacterial properties

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.