80909-78-0

Basic information

• Product Name: 2-(4-bromophenyl)-2-methyloxirane
• Synonyms: 2-(4-Bromophenyl)-2-methyloxirane
• CAS NO: 80909-78-0
• Molecular Formula: C₉H₉BrO
• Molecular Weight: 213.0712
• Mol File: 80909-78-0.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 247.3°C at 760 mmHg
• Flash Point: 97.9°C
• Density: 1.489g/cm³
• Vapor Pressure: 0.0407mmHg at 25°C
• Refractive Index: 1.579
• CAS DataBase Reference: 2-(4-bromophenyl)-2-methyloxirane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-bromophenyl)-2-methyloxirane(80909-78-0)
• EPA Substance Registry System: 2-(4-bromophenyl)-2-methyloxirane(80909-78-0)

Safety Data

• Hazardous Substances Data: 80909-78-0(Hazardous Substances Data)

Usage

General Description

2-(4-bromophenyl)-2-methyloxirane is a chemical compound with the molecular formula C9H9BrO. It is commonly used as a reagent in organic synthesis and is known for its ability to undergo ring-opening reactions with various nucleophiles. The compound contains a bromine atom and a phenyl group attached to a two-carbon oxirane ring, giving it a unique combination of reactivity and potential applications. It is important to handle this compound with care, as it is classified as a hazardous material and should only be used by trained professionals in a controlled laboratory setting.

Upstream product

• 98815-49-7 1-bromo-2-(4-bromophenyl)propan-2-ol 
• 75-16-1 methylmagnesium bromide 
• 99-73-0 para-bromophenacyl bromide 
• 6888-79-5 4-bromo-α-methylstyrene 
• 2181-42-2 trimethylsulphonium iodide 
• 99-90-1 para-bromoacetophenone 
• 6814-64-8 methylenedimethyl sulfurane 
• 2077-19-2 2-(4-bromophenyl)propan-2-ol 
• 1774-47-6 trimethylsulfoxonium iodide 
• 75-11-6 diiodomethane 

Downstream Products

• 1188337-28-1 2-(4-bromo-phenyl)-2-methyl-6-nitro-2,3-dihydro-imidazo[2,1-b]oxazole 
• 1239766-99-4 (R)-1-azido-2-(4-bromophenyl)propan-2-ol 
• 1239767-07-7 C₉H₁₀BrN₃O 
• 1239766-89-2 1-azido-2-(4-bromophenyl)propan-2-ol 
• 1304668-78-7 (R)-di-tert-butyl 1-(2-(4-bromophenyl)-1-oxo-propan-2-yl)hydrazine-1,2-dicarboxylate 
• 99-90-1 para-bromoacetophenone 
• 1188918-58-2 (R)-3-[2-fluoro-4'-(2-methyl-6-nitro-2,3-dihydro-imidazo[2,1-b]oxazol-2-yl)-biphenyl-4-yl]-5-hydroxymethyl-oxazolidin-2-one 
• 156143-00-9 (S)-(+)-2-(4'-bromophenyl)propanoic acid 
• 53086-53-6 2-(4-bromophenyl)propionic acid 
• 81310-74-9 4-bromo-α-methyl-benzeneethanol 
• 1612764-01-8 4-[4-[1-hydroxy-1-methyl-2-(1,2,4-triazol-1-yl)ethyl]phenoxy]benzonitrile 
• 1612764-19-8 2-(4-bromophenyl)-1-(1,2,4-triazol-1-yl)propan-2-ol 
• 1548513-39-8 C₁₁H₉BrO₂ 
• 40460-91-1 2-(4-bromophenyl)propanal 

Relevant articles and documents

Chemical space exploration of oxetanes

This paper focuses on new derivatives bearing an oxetane group to extend accessible chemical space for further identification of kinase inhibitors. The ability to modulate kinase activity represents an important therapeutic strategy for the treatment of h

Mild Iridium-Catalysed Isomerization of Epoxides. Computational Insights and Application to the Synthesis of β-Alkyl Amines

The isomerization of epoxides to aldehydes using the readily available Crabtree's reagent is described. The aldehydes were transformed into synthetically useful amines by a one-pot reductive amination using pyrrolidine as imine-formation catalyst. The reactions worked with low catalyst loadings in very mild conditions. The procedure is operationally simple and tolerates a wide range of functional groups. A DFT study of its mechanism is presented showing that the isomerization takes place via an iridium hydride mechanism with a low energy barrier, in agreement with the mild reaction conditions. (Figure presented.).

SUBSTITUTED [1,2,4]TRIAZOLE COMPOUNDS AND THEIR USE AS FUNGICIDES

The present invention relates to compoundsof the formula (I) wherein the variables are defined in the description and claims, their preparation and uses thereof.