1191925-09-3

Basic information

• Product Name: 5-bromomethyl-3-(p-toluyl)-Δ2-isoxazoline
• Synonyms: 5-bromomethyl-3-(p-toluyl)-Δ2-isoxazoline
• CAS NO: 1191925-09-3
• Molecular Weight: 254.126
• Mol File: 1191925-09-3.mol

Chemical Properties

• CAS DataBase Reference: 5-bromomethyl-3-(p-toluyl)-Δ2-isoxazoline(CAS DataBase Reference)
• NIST Chemistry Reference: 5-bromomethyl-3-(p-toluyl)-Δ2-isoxazoline(1191925-09-3)
• EPA Substance Registry System: 5-bromomethyl-3-(p-toluyl)-Δ2-isoxazoline(1191925-09-3)

Safety Data

• Hazardous Substances Data: 1191925-09-3(Hazardous Substances Data)

Upstream product

• 904672-45-3 1-(p-tolyl)-3-buten-1-one oxime 
• 104-87-0 4-methyl-benzaldehyde 
• 24165-63-7 1-p-tolyl-3-buten-1-ol 
• 130649-66-0 1-(4-Methylphenyl)-3-buten-1-one 

Relevant articles and documents

5-Bromomethyl-4,5-dihydroisoxazoles

The preparation of substituted 4,5-dihydroisoxazoles can be accomplished via the treatment of β,γ-unsaturated oximes with liquid bromine. The reaction provides a convenient route to the highly functionalized title compounds.

General 5-Halomethyl Isoxazoline Synthesis Enabled by Copper-Catalyzed Oxyhalogenation of Alkenes

A general and efficient oxyhalogenation of unsaturated ketoximes has been achieved through copper catalysis with diethyl bromomalonate, N-chlorosuccinimide, and N-iodosuccinimide, yielding 5-chloromethyl, 5-bromomethyl, and 5-iodomethyl isoxazolines in go

Synthesizing method of halogenated isoxazoline type compound

The invention discloses a synthesizing method of a halogenated isoxazoline type compound, and belongs to the field of organic synthesis. According to the synthesizing method, under the inert gas protection condition, a ketoxime type compound and an organi

Transition-metal-free oxychlorination of alkenyl oximes:: In situ generated radicals with tert -butyl nitrite

Oxychlorination of alkenyl oximes is harder compared to the analogous oxybromination or oxyiodination because of the difficulty associated with the formation of chlorine cations or radicals. A transition-metal-free oxychlorination of alkenyl oximes has be

Oxime-mediated oxychlorination and oxybromination of unactivated olefins

An oxime-mediated oxychlorination and oxybromination of unactivated olefins relying on palladium catalysis has been developed. A wide range of chlorinated and brominated isoxazolines has been synthesized in moderate to good yields. To demonstrate the value of the method, the brominated isoxazoline has been further converted to other useful synthetic feedstock.