2552-45-6

Usage

Uses

Used in Chemical Synthesis:
METHYL 4-CHLORO-3,5-DINITROBENZOATE is used as a precursor for the synthesis of other organic compounds, playing a crucial role in the creation of various chemical products.
Used in Dye Manufacturing:
In the dye industry, METHYL 4-CHLORO-3,5-DINITROBENZOATE is used as a key component in the manufacturing process, contributing to the development of different types of dyes.
Used in Pharmaceutical Production:
METHYL 4-CHLORO-3,5-DINITROBENZOATE is also utilized in the pharmaceutical sector, where it serves as a vital ingredient in the production of certain drugs.
Safety Note:
METHYL 4-CHLORO-3,5-DINITROBENZOATE is a hazardous chemical, and it is essential to handle it with care and in accordance with proper safety protocols to ensure the safety of individuals and the environment.

InChI:InChI=1/C8H5ClN2O6/c1-17-8(12)4-2-5(10(13)14)7(9)6(3-4)11(15)16/h2-3H,1H3

Upstream product

• 186581-53-3 diazomethane 
• 118-97-8 4-chloro-3,5-dinitrobenzoic acid 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 74-11-3 para-chlorobenzoic acid 
• 67-56-1 methanol 
• 42486-87-3 3,5-dinitro-4-chlorobenzenecarboxylic acid chloride 
• 33927-05-8 methyl 3,5-dinitro-4-hydroxybenzoate 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 33927-08-1 4-(4-methoxy-phenoxy)-3,5-dinitro-benzoic acid methyl ester 
• 108621-37-0 4-(2-methoxy-phenoxy)-3,5-dinitro-benzoic acid methyl ester 
• 911429-32-8 3-(4-methoxycarbonyl-2,6-dinitrophenyl)indole 
• 1202159-49-6 C₁₇H₁₅N₃O₆ 
• 1202159-48-5 C₁₅H₁₉N₃O₆ 
• 77762-28-8 4-methylamino-3,5-dinitro-benzoic acid methyl ester 
• 642068-72-2 methyl 3-amino-4-chloro-5-nitrobenzoate 
• 100146-11-0 4-(5,6-dimethoxy-3-oxo-phthalan-4-yloxy)-3,5-dinitro-benzoic acid methyl ester 
• 150272-18-7 4-[Bis-(2-hydroxy-ethyl)-amino]-3,5-dinitro-benzoic acid methyl ester 
• 52118-95-3 4-(2,4-Dibrom-6-methylphenoxy)-3,5-dinitrobenzoesaeuremethylester 
• 23501-52-2 2,3-Bis-<4-methoxycarbonyl-2,6-dinitro-phenoxy>-toluol (3-Methyl-2-<4-methoxy-carbonyl-2,6-dinitro-phenoxy>-4'-methoxycarbonyl-2',6'-dinitro-diphenylaether) 
• 23501-54-4 2,3-Bis-<4-methoxycarbonyl-2,6-dinitro-phenoxy>-naphthalin (4,5-Benzo-2-<4-me-thoxy-carbonyl-2,6-dinitro-phenoxy>-4'-methoxycarbonyl-2',6'-dinitro-diphenyl-aether) 
• 23501-53-3 3-Hydroxy-2-<4-methoxycarbonyl-2,6-dinitro-phenoxy>-naphthalin (4,5-Benzo-2-hydroxy-4'-methoxycarbonyl-2',6'-dinitro-diphenylaether) 
• 23501-55-5 2-<4-Methoxycarbonyl-2,6-dinitro-phenoxy>-fluoren 

Relevant academic research and scientific papers

HIGHLY ACTIVE STING PROTEIN AGONIST COMPOUND

The present invention provides compounds of Formula (I) or (II), pharmaceutical compositions thereof, and methods of using compounds of Formula (I) or (II) to prevent and/or treat immune-related disorders.

ANTI-INFECTIVE HETEROCYCLIC COMPOUNDS AND USES THEREOF

The present invention relates to heterocyclic compounds of Formula I useful as anti-infective agents. The present invention further relates to a method of treating an infection by administering such compounds, and to pharmaceutical compositions comprising such compounds.

DENDRITIC COMPOUNDS INCLUDING A CHELATING, FLUOROCHROME OR RECOGNITION AGENT, COMPOSITIONS INCLUDING SAME AND USES THEREOF

The invention relates to dendritic compounds comprising a chelating, fluorochrome or recognition agent of formula (I), to compositions comprising same, and to uses thereof, wherein in said formula (I): T, L1, D, R, L2, V and n are as defined in the description.

Second generation of BACE-1 inhibitors part 2: Optimisation of the non-prime side substituent

Our first generation of hydroxyethylamine transition-state mimetic BACE-1 inhibitors allowed us to validate BACE-1 as a key target for Alzheimer's disease by demonstrating amyloid lowering in an animal model, albeit at rather high doses. Finding a molecul

Discovery and optimization of antibacterial AccC inhibitors

The biotin carboxylase (AccC) is part of the multi-component bacterial acetyl coenzyme-A carboxylase (ACCase) and is essential for pathogen survival. We describe herein the affinity optimization of an initial hit to give 2-(2-chlorobenzylamino)-1-(cyclohe

Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators

The invention provides for a compound of formula (I) or a pharmaceutically acceptable salt thereof: wherein R1, R2, R3, A, B, D, m, n, x, and y are defined as described in the specification. The invention additionally provides a pharmaceutically composition comprising the compound of formula I, together with a method of using the same to treat or prevent neurological and psychiatric disorders. The compounds are useful in therapy related to the treatment or prevention of mGluR2 receptor-mediated disorders.

Synthesis and antibacterial activity of some substituted 3-(aryl)- and 3-(heteroaryl)indoles

A synthesis of 3-(4-methoxycarbonyl-2,6-dinitrophenyl)indole, its 2,6-diamino analog, and 3-(2-amino-4-trifluoromethyl-6-nitrophenyl)indole is described. 4-(Trifluoromethyl)phenyl derivatives exhibit higher antibacterial potency than the former 4-(methoxy

Effects of ortho- and para-ring activation on the kinetics of S NAr reactions of 1-chloro-2-nitro- and 1-phenoxy-2-nitrobenzenes with aliphatic amines in acetonitrile

Rate constants are reported for reaction of 4-substituted 1-chloro-2,6-dinitrobenzenes 1, 6-substituted 1-chloro-2,4-dinitrobenzenes 2, and some of the corresponding 1-phenoxy derivatives, 3 and 4, with n-butylamine, pyrrolidine and pi-peridine in acetoni

HYDROXYETHYLAMINE DERIVATIVES FOR THE TREATMENT OF ALZHEIMER'S DISEASE

The present invention relates to novel hydroxyethylamine compounds of formula (I): (I) having Asp2 (-secretase, BACE1 or Memapsin) inhibitory activity, processes for their preparation, to compositions containing them and to their use in the treatment of diseases characterised by elevated-amyloid levels or-amyloid deposits, particularly Alzheimer's disease.

Synthesis of Polyfunctionalized Biphenyls as Intermediates for a New Class of Liquid Crystals

A series of hexa- and octasubstituted biphenyls containing halogen, amino, nitro, and propylthio substituents were prepared by metal-mediated convergent synthesis from halobenzene precursors. The Pd-assisted C-C coupling methods were ineffective in the fo