37836-80-9

Basic information

• Product Name: 4(3H)-Pyrimidinone, 2-(1-methylethoxy)-6-(trifluoromethyl)-
• Synonyms: 4(3H)-Pyrimidinone, 2-(1-methylethoxy)-6-(trifluoromethyl)-;2-isopropoxy-6-trifluoroMethyl-3H-pyriMidin-4-one
• CAS NO: 37836-80-9
• Molecular Formula: C₈H₉F₃N₂O₂
• Molecular Weight: 222
• Mol File: 37836-80-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 191.8±50.0 °C(Predicted)
• Appearance: /
• Density: 1.40±0.1 g/cm3(Predicted)
• PKA: 6.17±0.50(Predicted)
• CAS DataBase Reference: 4(3H)-Pyrimidinone, 2-(1-methylethoxy)-6-(trifluoromethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4(3H)-Pyrimidinone, 2-(1-methylethoxy)-6-(trifluoromethyl)-(37836-80-9)
• EPA Substance Registry System: 4(3H)-Pyrimidinone, 2-(1-methylethoxy)-6-(trifluoromethyl)-(37836-80-9)

Safety Data

• Hazardous Substances Data: 37836-80-9(Hazardous Substances Data)

Usage

General Description

4(3H)-Pyrimidinone, 2-(1-methylethoxy)-6-(trifluoromethyl)- is a chemical compound with the molecular formula C11H11F3N2O2. It is a pyrimidinone derivative and contains a trifluoromethyl group, which is known for its electron-withdrawing properties. 4(3H)-Pyrimidinone, 2-(1-methylethoxy)-6-(trifluoromethyl)- has potential applications in the pharmaceutical industry due to its ability to interact with biological targets. It may be used as a building block in the synthesis of various drugs or as a pharmacophore in the design of new pharmaceutical agents. Additionally, the presence of the methylethoxy group may contribute to its solubility and bioavailability, making it a promising candidate for further drug development research.

Upstream product

• 28811-41-8 o-isopropylisourea hydrochloride 
• 372-31-6 ethyl 4,4,4-trifluoroacetoacetate 

Downstream Products

• 178813-81-5 fluacrypyrim 
• 178813-81-5 methyl 3-methoxy-2-(2-((2-isopropoxy-6-trifluoromethylpyrimidine-4-yl)oxymethyl)-phenyl)-acrylate 

Relevant articles and documents

2-?(2-Alkoxy-6-trifluoromethylpyrimidin-4-yl)oxymethylene!phenylacetic acid derivatives, their preparation and intermediate therefor, and use thereof

2-?(2-Alkoxy-6-trifluoromethylpyrimidin-4-yl)oxymethylene!-phenylacetic acid derivatives of the formula I STR1 where the index and the substituents have the following meanings: U is CH or N; V is O or NH; R is alkyl; R1 is cyano, halogen, alkyl