13335-73-4

Usage

Uses

Used in Agricultural Industry:
3,4-DIMETHYLPHENOXYACETIC ACID is used as a herbicide for controlling the growth of unwanted weeds in crops such as wheat, barley, and grapes. Its application helps to increase the yield of the desired plants by disrupting the normal growth and development processes of weeds.
3,4-DIMETHYLPHENOXYACETIC ACID is also used as a plant growth regulator to enhance the growth and productivity of crops. By mimicking the plant hormone auxin, it influences various physiological processes, contributing to improved crop performance.
However, it is important to note that the long persistence of 3,4-DIMETHYLPHENOXYACETIC ACID in soil and water may have potential implications for human health and the environment. Therefore, its application should be carefully managed and monitored to minimize any adverse effects.

InChI:InChI=1/C10H12O3/c1-7-3-4-9(5-8(7)2)13-6-10(11)12/h3-5H,6H2,1-2H3,(H,11,12)

Upstream product

• 95-65-8 3,4-Dimethylphenol 
• 79-11-8 chloroacetic acid 
• 79-08-3 bromoacetic acid 
• 95450-81-0 (3,4-dimethyl-phenoxy)-acetic acid methyl ester 
• 192634-75-6 ethyl [(3,4-dimethylphenyl)oxy]acetate 

Downstream Products

• 95450-81-0 (3,4-dimethyl-phenoxy)-acetic acid methyl ester 
• 82326-46-3 2-(3,4-Dimethyl-phenoxymethyl)-1H-benzoimidazole 
• 34279-10-2 3-[1-(3,4-Dimethyl-phenoxy)-meth-(Z)-ylidene]-3H-isobenzofuran-1-one 
• 1107603-71-3 C₂₅H₃₇NO₅ 
• 1107603-72-4 C₂₅H₃₇NO₅ 
• 1440434-98-9 N-(4-(3-chlorophenyl)thiazol-2-yl)-2-(3,4-dimethylphenoxy)acetamide 
• 1440434-94-5 2-(3,4-dimethylphenoxy)-N-(4-(3-fluorophenyl)thiazol-2-yl)acetamide 
• 899270-46-3 2-(3,4-dimethylphenoxy)-N-(4-methylthiazol-2-yl)acetamide 
• 123216-99-9 5-{[(3,4-dimethylphenyl)oxy]methyl}-1,3,4-thiadiazol-2-amine 

Relevant academic research and scientific papers

5,6,7,8-TETRAHYDRO-IMIDAZO[1,5-A]PYRAZINE DERIVATIVES

The invention relates to 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine derivatives of formula (I),wherein X represents CH2 or O; R1 represents a phenyl group, which group is independently mono-, di-, or tri-substituted wherein the substituents are independently selected from the group consisting of (C1-4)alkyl, (C1-4)alkoxy, halogen, cyano, trifluoromethoxy and trifluoromethyl; R2 represents (C1-4)alkyl, (C1-4)alkoxy, (C2-4)alkenyl, halogen, cyano, hydroxymethyl, trifluoromethyl, C(O)NR5R6 or cyclopropyl; R3 represents (C1-4)alkyl, (C1-4)alkoxy-methyl or halogen; R4 represents (C1-4)alkyl; R5 represents hydrogen or (C1-4)alkyl; and R6 represents hydrogen or (C1-4)alkyl. The invention also relates to pharmaceutically acceptable salts of such compounds; and to the use of such compounds as medicaments; especially as orexin receptor antagonists.

THIADIAZOLE DERIVATIVES, INHIBITORS OF STEAROYL-COA DESATURASE

The present invention relates to substituted thiadiazole compounds of the formula (I) and pharmaceutically acceptable salts thereof, to pharmaceutical compositions containing them and their use in medicine. In particular, the invention relates to compounds for modulating SCD activity.

Synthesis and characterization of polyaniline salts with phenoxy acetic acids by emulsion polymerization

Polyaniline salts have been synthesized by chemical oxidative polymerization of aniline in the presence of phenoxy acetic acid and its two derivatives using emulsion method at room temperature and characterized by different techniques such as infrared, 1H and 13C NMR, UV-visible spectroscopy, SEM, wide angle X-ray diffractograms and conductivity measurements. These polyaniline salts have the desirable property of high solubility for processibility in solvents such as DMF, DMSO and a mixture of CHCl3 and acetone and they exhibit fairly good conductivity of ～ 3.0 × 10-3 S cm-1. The variations in solubility, conductivity and morphology with the protonating strength of the dopants are examined.

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.

Herbicidal compositions for killing weeds in vineyards

A composition for selective weed control in vineyards and orchards containing as active material at least one of the following compounds: STR1