25181-66-2

Usage

Uses

Used in Agricultural Industry:
(2-BROMO-4-METHYLPHENOXY)ACETIC ACID is used as a plant growth regulator for the control of nut grass and oxalis. It helps in managing the growth of these invasive plants, which can be detrimental to the growth and health of other crops. By regulating the growth of these unwanted plants, (2-BROMO-4-METHYLPHENOXY)ACETIC ACID contributes to improved crop yield and overall agricultural productivity.

InChI:InChI=1/C9H9BrO3/c1-6-2-3-8(7(10)4-6)13-5-9(11)12/h2-4H,5H2,1H3,(H,11,12)

Upstream product

• 6627-55-0 2-bromo-p-cresol 
• 79-08-3 bromoacetic acid 
• 79-11-8 chloroacetic acid 
• 1240286-85-4 tert-butyl (2-bromo-4-methylphenoxy)acetate 
• 105-36-2 ethyl bromoacetate 
• 940-64-7 2-(4-methylphenoxy)acetic acid 

Downstream Products

• 904297-94-5 benzoic acid N'-[2-(2-bromo-4-methyl-phenoxy)-acetyl]-N'-isopropyl-hydrazide 
• 203571-86-2 (2-Bromo-4-methyl-phenoxy)-acetyl chloride 

Relevant academic research and scientific papers

Design, synthesis and biological evaluation of oxime lacking Psammaplin inspired chemical libraries as anti-cancer agents

In this study, we attempted the chemical simplification of Psammaplin (PsA), while retaining its activity in vitro. Inspired by the previous Structure Activity Relationship (SAR) studies on various PsA analogues and relying on the fact that oxime is metabolically unstable, we initially designed and synthesized a diverse library of PsA analogues and evaluated for cytotoxic activity. Among 32 compounds of Psammaplin analogues synthesized, the compound 10b was almost equally active as parent Psammaplin in vitro.

Diacylglycerol acyltransferase inhibitors

Provided herein are compounds of the formula (1): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity, type II diabetes mellitus and metabolic syndrome.

Heterocyclically Bridged Tricyclic β-Lactames: A Simple Synthesis of 1,2,2a,8a-Tetrahydro-3-oxa-1-aza-cyclobuta[b]naphthalen-2-ones

The tricylic 3,4-bridged β-lactames 7 and 8 containing a hetero atom as 3-substituent of the azetidin-2-one ring were synthesized by intramolecular radical cyclization using cis-substituted 3-(2-bromo-aryloxy)-azetidine-2-ones 6 as precursors. These precu

Design, Synthesis, and Testing of Potential Antisickling Agents. 4. Structure-Activity Relationships of Benzyloxy and Phenoxy Acids

In this paper we further establish the activity of two classes of small molecules, benzyloxy and phenoxy acids, as potent inhibitors of hemoglobin S (HbS) gelation.Structural modifications with a large number of each class confirm our earlier work that the highest activity is observed with compounds that contain dihalogenated aromatic rings with attached polar side chains.We have also found a halogenated aromatic malonic acid derivative to be quite active.Compounds reported in this paper are compared with other antigelling agents studied in our laboratory.Comments are made concerning the antigelling activity and binding sites of four derivatives and their effect on the allosteric mechanism of hemoglobin (Hb) function.