69033-87-0

Basic information

• Product Name: 5-BROMO-2-(4-METHOXYPHENOXY)PYRIMIDINE
• Synonyms: 5-BROMO-2-(4-METHOXYPHENOXY)PYRIMIDINE
• CAS NO: 69033-87-0
• Molecular Formula: C₁₁H₉BrN₂O₂
• Molecular Weight: 281.10536
• Mol File: 69033-87-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 408.4°C at 760 mmHg
• Flash Point: 200.8°C
• Appearance: /
• Density: 1.506g/cm³
• Vapor Pressure: 1.66E-06mmHg at 25°C
• Refractive Index: 1.592
• CAS DataBase Reference: 5-BROMO-2-(4-METHOXYPHENOXY)PYRIMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-2-(4-METHOXYPHENOXY)PYRIMIDINE(69033-87-0)
• EPA Substance Registry System: 5-BROMO-2-(4-METHOXYPHENOXY)PYRIMIDINE(69033-87-0)

Safety Data

• Hazardous Substances Data: 69033-87-0(Hazardous Substances Data)

Usage

General Description

5-Bromo-2-(4-methoxyphenoxy)pyrimidine is a chemical compound with the molecular formula C11H9BrN2O2. It is a pyrimidine derivative and contains a bromine atom and a methoxyphenyl group. This chemical is commonly used as a building block in the synthesis of various biologically active compounds, particularly in the field of medicinal chemistry. It has been studied for its potential pharmaceutical applications, particularly as a modulator of biological pathways and as a potential therapeutic agent. 5-Bromo-2-(4-methoxyphenoxy)pyrimidine is commonly used in research and has shown promise in various applications due to its unique chemical structure and potential biological activities.

InChI:InChI=1/C11H9BrN2O2/c1-15-9-2-4-10(5-3-9)16-11-13-6-8(12)7-14-11/h2-7H,1H3

Upstream product

• 5720-07-0 4-methoxyphenylboronic acid 
• 38353-06-9 5-bromo-1H-pyrimidin-2-one 
• 150-76-5 4-methoxy-phenol 
• 32779-36-5 5-Bromo-2-chloropyrimidine 

Downstream Products

• 1147704-28-6 1-(4-(2-(4-methoxyphenoxy)pyrimidin-5-yl)phenyl)ethanone 
• 1147704-29-7 methyl 4-(2-(4-methoxyphenoxy)pyrimidin-5-yl)benzoate 
• 1147704-27-5 2-(4-methoxyphenoxy)-5-phenylpyrimidine 
• 69033-88-1 4-(5-bromo-pyrimidin-2-yloxy)-phenol 

Relevant articles and documents

One-pot etherification of purine nucleosides and pyrimidines

A one-pot synthesis of ethers derived from inosine, guanosine, 2′-deoxyguanosine, and pyrimidinones is described. Exposure of the heterocycle to 1H-benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and Cs2CO3/s

Hydrogen peroxide mediated formation of heteroaryl ethers from pyridotriazol-1-yloxy heterocycles and arylboronic acids

Pyridotriazol-1-yloxypyrimidine 3 reacts with arylboronic acids under palladium-free, Cs2CO3, (0.8%) H2O2, and DME conditions to produce heteroaryl ethers 4-16 in good yields comparable to the oxidative palladiu

Derivatives of (pyrimidyloxy)phenoxy-alkanecarboxylic acid and herbicidal compositions thereof

A compound of general formula I: STR1 wherein A, B, D, E, and V are independently chosen from hydrogen, halogen, nitro, cyano, thiocyano, amino, alkyl, alkoxy, alkylthio, alkenyl, cycloalkyl, carbalkoxy, phenyl, phenoxy or phenylthio; R1 and R2 are independently hydrogen, alkyl, alkenyl, alkanoyl, or R1 and R2 together are alkylidene; W is carboxy or a functional derivative thereof or CH2 Z wherein Z is halogen, hydroxy, alkoxy, alkylthio, formyl or amino; and X and Y are oxygen or sulfur.