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2,6-Dichloro-N,N-diethylpyrimidin-4-amine, with the molecular formula C10H15Cl2N3, is a chemical compound that serves as an effective herbicide in agricultural applications. It functions by inhibiting the enzyme dihydropteroate synthase, which is crucial for the synthesis of tetrahydrofolic acid, a vital component for plant growth. This action leads to the suppression of targeted weed growth, making it a valuable tool for enhancing crop yields.

78418-15-2

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78418-15-2 Usage

Uses

Used in Agricultural Industry:
2,6-Dichloro-N,N-diethylpyrimidin-4-amine is used as a herbicide for weed control in agricultural crops. It is applied to inhibit the growth of unwanted plants by targeting their essential enzyme dihydropteroate synthase, thereby disrupting the synthesis of tetrahydrofolic acid and suppressing their growth. This contributes to improved crop yields and reduced competition for resources among plants.
It is important to handle 2,6-Dichloro-N,N-diethylpyrimidin-4-amine with care due to its potential harmful effects if ingested or inhaled, as well as its negative impacts on aquatic life. Proper management and application protocols are essential to ensure the safety of both humans and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 78418-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,1 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78418-15:
(7*7)+(6*8)+(5*4)+(4*1)+(3*8)+(2*1)+(1*5)=152
152 % 10 = 2
So 78418-15-2 is a valid CAS Registry Number.

78418-15-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichloro-N,N-diethylpyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names N-(2,6-Dichloropyrimidin-4-yl)diethylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:78418-15-2 SDS

78418-15-2Relevant academic research and scientific papers

Synthesis and biological evaluation of novel pyrimidine derivatives as sub-micromolar affinity ligands of GalR2

Sagi, Vasudeva Naidu,Liu, Tianyu,Lu, Xiaoying,Bartfai, Tamas,Roberts, Edward

scheme or table, p. 7210 - 7215 (2012/01/15)

GalR1 and GalR2 represent unique pharmacological targets for treatment of seizures and epilepsy. A novel series of 2,4,6-triaminopyrimidine derivatives were synthesized and found to have sub-micromolar affinity for GalR2. Optimization of a series of 2,4,6

HETEROARYL COMPOUNDS

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Page/Page column 99-100, (2010/11/30)

This invention relates to compounds of formula (I) their compositions and methods of use thereof. The compounds (and compositions) are useful in modulating IL-12 production and processes mediated by IL-12.

Simplified analogues of acyclonucleosides. Synthesis of 6-[N-alkyl-N-(4- hydroxybutyl)amino]pyrimidine derivatives

Botta,Saladino,Anzini,Corelli

, p. 1769 - 1777 (2007/10/02)

The synthesis of some 6-alkylaminopyrimidine derivatives bearing a 4- hydroxybutyl chain as sugar mimic is described. These new compounds can be regarded as simplified, ring-opened analogues of purine acyclonucleosides.

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