1373930-83-6

Basic information

• Product Name: methyl (E)-2-({4-bromo-2-[(E)-(hydroxyimino)methyl]phenoxy}methyl)-3-(p-tolyl)acrylate
• Synonyms: methyl (E)-2-({4-bromo-2-[(E)-(hydroxyimino)methyl]phenoxy}methyl)-3-(p-tolyl)acrylate
• CAS NO: 1373930-83-6
• Molecular Weight: 404.26
• Mol File: 1373930-83-6.mol

Chemical Properties

• CAS DataBase Reference: methyl (E)-2-({4-bromo-2-[(E)-(hydroxyimino)methyl]phenoxy}methyl)-3-(p-tolyl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (E)-2-({4-bromo-2-[(E)-(hydroxyimino)methyl]phenoxy}methyl)-3-(p-tolyl)acrylate(1373930-83-6)
• EPA Substance Registry System: methyl (E)-2-({4-bromo-2-[(E)-(hydroxyimino)methyl]phenoxy}methyl)-3-(p-tolyl)acrylate(1373930-83-6)

Safety Data

• Hazardous Substances Data: 1373930-83-6(Hazardous Substances Data)

Upstream product

• 139413-76-6 methyl (2Z)-2-(bromomethyl)-3-(4-methylphenyl)prop-2-enoate 
• 1761-61-1 5-bromosalicyclaldehyde 
• 1373930-71-2 C₁₉H₁₇BrO₄ 

Relevant articles and documents

Intramolecular 1,3-dipolar nitrile oxide cycloaddition using Baylis-Hillman derivatives: Stereoselective synthesis of tricyclic chromenoisoxazolines

A novel protocol for the construction of tricyclic chromenoisoxazoline frameworks via an intramolecular 1,3-dipolar nitrile oxide cycloaddition (INOC) reaction using Baylis-Hillman derivatives is described for the first time. The INOC reaction leads to a