58-81-1

Basic information

• Product Name: 2,4,6-Trichloro-5-n-propylpyriMidine, 96%
• Synonyms: 2,4,6-Trichloro-5-n-propylpyriMidine, 96%
• CAS NO: 58-81-1
• Molecular Formula: C₇H₇Cl₃N₂
• Molecular Weight: 225.50288
• Mol File: 58-81-1.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4,6-Trichloro-5-n-propylpyriMidine, 96%(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Trichloro-5-n-propylpyriMidine, 96%(58-81-1)
• EPA Substance Registry System: 2,4,6-Trichloro-5-n-propylpyriMidine, 96%(58-81-1)

Safety Data

• Hazardous Substances Data: 58-81-1(Hazardous Substances Data)

Usage

General Description

2,4,6-Trichloro-5-n-propylpyriMidine, 96% is a chemical compound that is commonly used as a pesticide and herbicide. It belongs to the class of pyrimidine compounds and is a potent inhibitor of photosynthesis in plants. Its 96% purity indicates that it is a highly concentrated form of the compound, making it effective at low concentrations. The trichloro and propyl groups on the pyrimidine ring give the compound its herbicidal properties, making it a valuable tool for controlling unwanted plant growth in agricultural and industrial settings. However, care must be taken when handling and using this chemical, as it can be toxic to humans and other animals.

Upstream product

• 2163-48-6 diethyl propylmalonate 
• 6156-88-3 5-propyl-barbitursaeure 

Downstream Products

• 120268-59-9 C₃₄H₃₂N₂O₉ 
• 1310053-28-1 6-(4-phenyl-1-piperazinyl)-5-(n-propyl)uracil 
• 1310053-29-2 6-[4-(2-methoxyphenyl)-1-piperazinyl]-5-(n-propyl)uracil 
• 1310053-30-5 6-[4-(3-trifluoromethylphenyl)-1-piperazinyl]-5-(n-propyl)uracil 

Relevant articles and documents

Synthesis and antimicrobial activity of some novel 5-alkyl-6-substituted uracils and related derivatives

6-Chloro-5-ethyl-, n-propyl- and isopropyluracils 5a-c were efficiently prepared from the corresponding 5-alkybarbituric acids 3a-c via treatment with phosphorus oxychloride and N,N-dimethylaniline to yield the corresponding 5-alkyl-2,4,6-trichloropyrimidines 4a-c, which were selectively hydrolyzed by heating in 10% aqueous sodium hydroxide for 30 minutes. The reaction of compounds 5a-c with 1-substituted piperazines yielded the corresponding 5-alkyl-6-(4-substituted-1-piperazinyl)uracils 6a-j. The target 8-alkyltetrazolo[1,5-f]pyrimidine-5,7(3H,6H)-diones 7a-c were prepared via the reaction of 5a-c with sodium azide. Compounds 6a-j and 7a-c were tested for in vitro activities against a panel of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Compound 6h displayed potent broad-spectrum antibacterial activity, while compound 6b showed moderate activity against the Gram-positive bacteria. All the tested compounds were practically inactive against Candida albicans.