21436-96-4

Usage

Uses

Used in Pharmaceutical Industry:
2,4-Dimethylaniline hydrochloride is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drug molecules.
Used in Agrochemical Industry:
It serves as a precursor in the production of agrochemicals, playing a crucial role in the creation of compounds that protect crops and enhance agricultural productivity.
Used in Pigment Industry:
2,4-Dimethylaniline hydrochloride is utilized as a component in the formulation of pigments, contributing to the coloration and stability of various products.
Used in Organic Chemistry Research:
As a reagent, 2,4-Dimethylaniline hydrochloride is employed in organic chemistry reactions to facilitate specific transformations and syntheses of target compounds.
Used in Polymer Synthesis:
It acts as a precursor in the synthesis of various polymers, which are then used in a wide range of applications, including plastics, coatings, and textiles.
It is important to handle 2,4-Dimethylaniline hydrochloride with care due to its potential harmful effects if ingested, inhaled, or in contact with the skin, emphasizing the need for proper safety measures during its use in various industries.

InChI:InChI=1/C8H11N.ClH/c1-6-3-4-8(9)7(2)5-6;/h3-5H,9H2,1-2H3;1H

Upstream product

• 95-68-1 2,4-Xylidine 

Downstream Products

• 88-05-1 2,4,6-trimethylaniline 
• 112677-30-2 1-(2,4-xylyl)guanidine 
• 16738-20-8 (2,4-dimethylphenyl)thiourea 
• 88565-88-2 4,6,8-trimethylquinoline 
• 28510-45-4 1-(2,4-dimethyl-phenyl)-biguanide 
• 16596-04-6 N,N'-bis-(2,4-dimethyl-phenyl)-formamidine 
• 159267-25-1 2,4-dimethylanilinium trichlorostannate(II) 
• 1200835-88-6 C₁₁H₁₅N₅O₂ 
• 1200835-67-1 1-((6-chloropyridin-3-yl)methyl)-5-(2,4-dimethylphenyl)-1,3,5-hexahydrotriazine-2-(N-nitro)imine 
• 96983-10-7 2,2-dimethyl-butyric acid-(2,4-dimethyl-anilide) 
• 60397-77-5 N-(2,4-dimethylphenyl)formamide 
• 73568-31-7 2-chloro-6,8-dimethylquinoline-3-carbaldehyde 
• 462067-46-5 C₁₄H₁₈N₂O₂ 
• 2050-43-3 N-(2,4-dimethylphenyl)acetamide 

Relevant academic research and scientific papers

METAL COMPLEX, COMPOSITION AND LIGHT EMITTING DEVICE

A metal complex represented by formula (1) is provided. In formula (1), X represents a nitrogen atom or a group represented by ═C(RX)—; R1 represents an alkyl group having 4 or more carbon atoms; R2 represents an alkyl, cycloalkyl, alkoxy, cycloalkoxy, aryl, aryloxy, monovalent heterocyclic, or substituted amino group or a halogen atom; rings A and B each independently represent an aromatic hydrocarbon ring or an aromatic heterocyclic ring; M represents a rhodium, palladium, iridium, or platinum atom; n1 represents an integer of 1 or more, n2 represents an integer of 0 or more, and n1+n2 is 2 or 3; A1-G1-A2 represents an anionic bidentate ligand; A1 and A2 each independently represent a carbon atom, an oxygen atom, or a nitrogen atom; and G1 represents a single bond or an atomic group constituting a bidentate ligand together with A1 and A2.

Synthesis, insecticidal activities, and molecular docking studies of 1,5-disubstituted-1,3,5-hexahydrotriazine-2-(N-nitro)imines

Figure represented. A series of novel neonicotinoids analogs were designed by modifying the pharmacophore of imidacloprid to 1,3,5-hexahydrotriazine conjugated to nitroimine (iNNO2) and introducing the phenyl or arylmethyl at the 5-position, and their insecticidal activities were evaluated. Introducing a heterocyclic methyl at 5-position increased the insecticidal activities, whereas other phenyl, phenylmethyl or phenylethyl substituents were unfavorable to activities. Molecular docking study was also performed to clarify the interactions of the most potent analog 1-((6-chloropyridin-3-yl)methyl)-5- (3-pyridylmethyl)-1,3,5-hexahydrotriazine-2-(N-nitro) imine (7s) with the target nicotinic acetylcholine receptor, which explained the structure-activity relationships observed in vitro, and revealed further possibilities for insecticide development.

Steric hindrance as a key factor on proton transfer in the σ-adduct forming reactions of o-substituted anilines with 1,3,5-trinitrobenzene in dimethylsulfoxide

Kinetic and equilibrium studies are reported of the reactions of 1,3,5-trinitrobenzene (TNB) with a series of o-substituted anilines in dimethyl sulfoxide (DMSO) in the presence of 1,4-diazabicyclo[2.2.2.]octane (DABCO). The pKa values in DMSO for the aniline derivatives were measured using the proton-transfer equilibrium with 2,4-dinitrophenol. Kinetic studies are compatible with a two-step process involving initial nucleophilic attack on TNB by amine to give a zwitterionic intermediate which may transfer an acidic proton to DABCO to yield the anionic product. The results indicate steric hindrance to proton transfer in reactions involving 2,6-disubstituted anilines.

Triazapentadienes as acaricides and insecticides

The preparation of triazapentadienes with acaricidal and insecticidal properties is described.