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78418-15-2

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78418-15-2 Usage

General Description

2,6-Dichloro-N,N-diethylpyrimidin-4-amine is a chemical compound with the molecular formula C10H15Cl2N3. It is commonly used as an herbicide, specifically in weed control for agricultural crops. 2,6-DICHLORO-N,N-DIETHYLPYRIMIDIN-4-AMINE works by inhibiting the enzyme dihydropteroate synthase, which is essential for the synthesis of tetrahydrofolic acid, an important component for the growth of plants. As a result, the growth of targeted weeds is suppressed, making it a valuable tool for agriculture. However, it is important to handle this chemical with care, as it can be harmful if ingested or inhaled, and can also have negative impacts on aquatic life.

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 articles and documents

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

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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