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1,3,5-Triazine-2,4-diamine, 6-chloro-N,N'-bis(2,4-dichlorophenyl)-, also known as atrazine desethyl, is a chemical compound derived from the parent compound atrazine. It is formed as a result of the metabolism of atrazine in the environment, particularly in plants and soil. 1,3,5-Triazine-2,4-diamine, 6-chloro-N,N'-bis(2,4-dichlorophenyl)- is a triazine-based herbicide that is widely used for controlling broadleaf and grassy weeds in various crops. It is characterized by its chemical structure, which includes a triazine ring with two amino groups at the 2 and 4 positions, a chloro group at the 6 position, and two 2,4-dichlorophenyl groups attached to the nitrogen atoms. Atrazine desethyl is known for its persistence in the environment and potential impact on aquatic ecosystems, leading to concerns about its use and the development of alternative herbicides with lower environmental impact.

2272-31-3

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2272-31-3 Usage

Type of compound

Chemical compound

Application

Herbicide

Usage

Control the growth of weeds in agricultural and horticultural settings

Mechanism of action

Inhibits photosynthesis in target plants

Combination use

Often used with other herbicides for broad-spectrum control

Toxicity

Moderately toxic to humans and animals

Handling precaution

Must be handled with caution to avoid harm

Check Digit Verification of cas no

The CAS Registry Mumber 2272-31-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2272-31:
(6*2)+(5*2)+(4*7)+(3*2)+(2*3)+(1*1)=63
63 % 10 = 3
So 2272-31-3 is a valid CAS Registry Number.

2272-31-3Downstream Products

2272-31-3Relevant academic research and scientific papers

Synthesis and biological evaluation of some new 3,4-dihydropyrimidin-4-ones

Modha, Jayesh,Datta, Neela,Parekh, Hansa

, p. 641 - 646 (2001)

Condensation of 5-cyano-2-hydrazino-3-N-methyl-6-phenyl/p-chlorophenyl-3,4-dihydropyrimidin-4 -one (3a and 3b) with 2,4-bisalkyl/arylamino-6-chloro-s-triazine (4) gave the corresponding 2,4-bisalkyl/arylamino-6-[5′-cyano-3′-N-methyl]-6′-phenyl/p -chlorophenyl-3′,4′-dihydropyrimidin-4′-one-2′-yl-hyd razino-s-triazines (5a-n and 6a-n). The compounds 4 have been prepared by the condensation of cyanuric chloride and different alkyl/aryl amines. The reaction between 5-cyano-3-N-methyl-2-methylthio-6-phenyl/p-chlorophenyl-3,4-dihydropyrimidin- 4-one (2a and 2b) with hydrazine hydrate furnished 3a and 3b, respectively. The condensation of 6-phenyl/p-chlorophenyl/5-cyano-2-mercapto-3,4-dihydropyrimidin-4-one (1a and 1b) with methyl iodide yielded 2a and 2b, respectively. All the products have been evaluated in vitro for their antimicrobial activity against several microbes and antitubercular activity against Mycobacterium tuberculosis H37 Rv. Copyright

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