1619228-51-1

Basic information

• Product Name: 2-bromo-1-(prop-1-en-2-yl)-3-(prop-2-yn-1-yloxy)cyclohex-1-ene
• Synonyms: 2-bromo-1-(prop-1-en-2-yl)-3-(prop-2-yn-1-yloxy)cyclohex-1-ene
• CAS NO: 1619228-51-1
• Molecular Weight: 255.155
• Mol File: 1619228-51-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-bromo-1-(prop-1-en-2-yl)-3-(prop-2-yn-1-yloxy)cyclohex-1-ene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-1-(prop-1-en-2-yl)-3-(prop-2-yn-1-yloxy)cyclohex-1-ene(1619228-51-1)
• EPA Substance Registry System: 2-bromo-1-(prop-1-en-2-yl)-3-(prop-2-yn-1-yloxy)cyclohex-1-ene(1619228-51-1)

Safety Data

• Hazardous Substances Data: 1619228-51-1(Hazardous Substances Data)

Upstream product

• 1619228-46-4 2-bromo-3-(prop-1-en-2-yl)cyclohex-2-en-1-one 
• 85493-96-5 2-bromo-3-methoxy-2-cyclohexenone 
• 1619228-48-6 2-bromo-3-(prop-1-en-2-yl)cyclohex-2-en-1-ol 
• 106-96-7 propargyl bromide 

Downstream Products

• 1619228-48-6 2-bromo-3-(prop-1-en-2-yl)cyclohex-2-en-1-ol 

Relevant articles and documents

Halogen effect on tandem [4+2] cycloaddition/aromatization sequence of allenyl 2-halo-3-vinylcyclohex-2-enyl ether

Steric and enthalpic effects of substituents on diene moieties play a crucial role in intramolecular cycloaddition reactions. Allenyl 2-halogenated-3-vinylcyclohex-2-enyl ethers underwent a tandem [4+2] cycloaddition/aromatization reaction to afford the corresponding tetrahydro-3H-naphtho[1,8-bc]furan compound in high yield.