1122-73-2

Usage

Uses

Used in Agricultural Industry:
2-AMINO-4-METHOXY-6-METHYL-1,3,5-TRIAZINE is used as a pre-emergent herbicide for controlling grasses and broadleaf weeds in various crops such as corn, soybeans, and sugarcane. It functions by inhibiting photosynthesis in plants, thereby disrupting their energy production process. Given its effectiveness in controlling unwanted plant growth, it plays a crucial role in enhancing crop yields and maintaining the health of agricultural fields.
Given the provided materials, there are no other specific applications mentioned for 2-AMINO-4-METHOXY-6-METHYL-1,3,5-TRIAZINE outside of its use in the agricultural industry. However, due to its chemical nature and properties, it may have potential uses in other areas such as chemical research or as an intermediate in the synthesis of other compounds, but these are not detailed in the provided information. It is important to handle and apply 2-AMINO-4-METHOXY-6-METHYL-1,3,5-TRIAZINE with care, adhering to safety guidelines to minimize environmental impact and ensure the safety of users.

InChI:InChI=1/C5H8N4O/c1-3-7-4(6)9-5(8-3)10-2/h1-2H3,(H2,6,7,8,9)

Upstream product

• 67-56-1 methanol 
• 7709-13-9 4-amino-2-chloro-1,3,5-triazine 
• 124-41-4 sodium methylate 
• 18871-66-4 N,N-dimethylacetamide dimethyl acetal 
• 869-75-0 amidino-O-methylisourea hydrochloride 

Relevant academic research and scientific papers

INHIBITORS OF CELLULAR METABOLIC PROCESSES

The invention provides inhibitor compounds of MAT2A that are useful as therapeutic agents for treating malignancies wherein the compounds have the general formula (I) : wherein ring A, ring B, ring C and, R1 are as described herein.

KONETICS OF THE REACTION OF GUANYL-O-METHYLISOUREA HYDROCHLORIDE WITH DIMETHYLFORMAMIDE DIMETHYLACETAL

The reaction of guanyl-O-methylisourea hydrochloride (IV) with dimethylformamide dimethylacetal (V) proceeds in two steps.The first step consists in the reaction of the imidoester with the imidatonium ion formed in a fast pre-equilibrium to give a conjugated system with the absorption maximum at 278 nm.The subsequent slower step consists in the cyclization to 2-amino-4-methoxy-1,3,5-triazine (VI).The rate of the first step is directly proportional to the concentrations of both hydrochloride IV and acetal V.Both the steps involve base catalysis.Mechanism of the whole reaction is suggested on the basis of the kinetic results.

PREPARATION OF SUBSTITUTED 5-PYRIMIDINECARBONITRILES AND 1,3,5-TRIAZINES FROM ALKYL N-CYANOIMIDATES

Sodium methoxide induced the cyclization of alkyl N-cyanoimidates 1 with propanedinitrile affording the 5-pyrimidinecarbonitriles 2.The reaction of 1 with methyl cyanoaetate led to the methyl 3-propenoates 7 and the 2,4-dioxo-5-pyrimidinecarbonitrile 8.An analogous cyclization of 1 with cyanamide yielded the 1,3,5-triazines 10.

4-Amino-2-chloro-1,3,5-triazine: A New Metabolite of Atrazine by a Soil Bacterium

The degradation of herbicide atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazine) by a soil bacterium is reported.The bacterium involved is a species of Nocardia, which utilizes the atrazine as the sole source of carbon and nitrogen.A new metabolite, 4-amino-2-chloro-1,3,5-triazine, of the degradation of atrazine in the presence of glucose has been identified.The results further substantiated that atrazine can be degraded by soil microorganisms and indicated that deamination can also occur, as well as dealkylation. 4-Amino-2-chloro-1,3,5-triazine did not show phytotoxic activity to oat (Avena sativa L.), demonstrating that deamination insures detoxification.