83141-02-0

Usage

Uses

Used in Pharmaceutical Industry:
2,6-Dichloro-3-nitrobenzyl bromide is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its reactivity allows for the creation of a wide range of drug molecules, making it a valuable component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical industry, 2,6-Dichloro-3-nitrobenzyl bromide serves as an intermediate in the production of various agrochemicals. Its ability to react with other compounds contributes to the development of effective pesticides and other agricultural products.
Used in Organic Synthesis:
2,6-Dichloro-3-nitrobenzyl bromide is utilized as a key intermediate in organic synthesis for creating a variety of organic compounds. Its versatility in reacting with different substances makes it an essential component in the synthesis of numerous organic molecules for various applications.

Upstream product

• 20443-98-5 2,6-Dichlorobenzyl bromide 
• 29682-46-0 2,6-dichloro-3-nitrotoluene 

Downstream Products

• 199849-80-4 4-(2,6-dichloro-3-nitro-benzyloxy)-benzothiazole 
• 167834-56-2 8-(2,6-Dichloro-3-nitro-benzyloxy)-2-methyl-quinoline 
• 82617-49-0 2-bromo-1-bromomethyl-3-nitrobenzene 
• 160647-05-2 8-(2,6-dichloro-3-nitrobenzyloxy)-2-methylimidazo[1,2-a]pyridine 
• 179625-53-7 8-(2,6-dichloro-3-aminobenzyloxy)-2-methylquinoline 
• 761448-10-6 2-(2,6-dichloro-3-nitro-benzyl)-isoindole-1,3-dione 
• 761448-13-9 {3-[3-(2-bromo-phenyl)-ureido]-6-chloro-2-hydroxy-benzyl}-carbamic acid tert-butyl ester 
• 761448-12-8 (6-chloro-2-hydroxy-3-nitro-benzyl)-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Discovery of potent and orally bioavailable N,N′-diarylurea antagonists for the CXCR2 chemokine receptor

A series of 3-substituted N,N′-diarylureas was prepared and CXCR2 receptor affinities as well as pharmacokinetic properties were examined. A series of 3-substituted N,N′-diarylureas was prepared and the structure-activity relationship relative to CXCR2 re

Novel heteroaryl alkylamide derivatives useful as bradykinin receptor modulators

This invention is directed towards novel alkylamide derivatives as bradykinin receptor antagonists useful for the treatment of bradykinin modulated disorders such as pain, inflammation, asthma and allergy. Furthermore, the present invention is directed to novel alkylamide derivatives as bradykinin receptor agonists useful for the treatment of bradykinin modulated disorders such as hypertension and the like.

NOVEL HETEROARYL ALKYLAMIDE DERIVATIVES USEFUL AS BRADYKININ RECEPTOR MODULATORS

This invention is directed towards novel alkylamide derivatives as bradykinin receptor antagonists useful for the treatment of bradykinin modulated disorders such as pain, inflammation, asthma and allergy. Furthermore, the present invention is directed to novel alkylamide derivatives as bradykinin receptor agonists useful for the treatment of bradykinin modulated disorders such as hypertension and the like.

Cyclic amine derivatives of substituted quinoxaline 2,3-diones as glutamate receptor antagonists

A novel series of substituted quinoxaline 2,3-diones useful as neuroprotective agents are taught. Novel intermediates, processes of preparation, and pharmaceutical compositions containing the compounds are also taught. The compounds are glutamate antagoni

Novel series of O-substituted 8-quinolines and 4-benzothiazoles as potent antagonists of the bradykinin B2 receptors

The synthesis and the SAR study of novel O-substituted 8-quinolines and 4-benzothiazoles as highly potent non-peptide bradykinin B2 receptor antagonists are described. Several members of this series of antagonists efficiently inhibited the BK-induced vasoconstriction on different isolated organ preparations.

Fluoroalkyl- and fluoroalkoxy-substituted heterocyclic bradykinin antagonists, process for their preparation, and their use

Fluoroalkyl- and fluoroalkoxy-substituted heterocyclic bradykinin antagonists, process or their preparation, and their useHeterocyclic fluoroalkyl derivatives and fluoroalkoxy derivatives of the formula (I) having bradykinin-antagonistic action STR1 in wh

3-(Pyrrol-1-yl)phenylmethyl esters and intermediates

3-(Pyrrol-1-yl)phenylmethyl esters and intermediates having the general formula STR1 the use of the esters as pesticides, compositions thereof and a process for preparation are disclosed and exemplified.