295324-71-9

Basic information

• Product Name: Benzene, (6-bromo-1-hexenyl)-
• CAS NO: 295324-71-9
• Molecular Formula: C12H15Br
• Molecular Weight: 239.155
• Mol File: 295324-71-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, (6-bromo-1-hexenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (6-bromo-1-hexenyl)-(295324-71-9)
• EPA Substance Registry System: Benzene, (6-bromo-1-hexenyl)-(295324-71-9)

Safety Data

• Hazardous Substances Data: 295324-71-9(Hazardous Substances Data)

Upstream product

• 98078-15-0 6-phenylhex-5-en-1-ol 
• 111-24-0 1,5-dibromo-pentane 
• 100-52-7 benzaldehyde 
• 34626-52-3 5-hydroxypentyltriphenylphosphonium bromide 

Downstream Products

• 1330074-89-9 C₂₁H₂₀ClNO 
• 3900-93-4 2-cyclopentyl-2-phenylacetic acid 
• 58007-86-6 C₂₄H₃₀ 
• 6111-82-6 1-phenylhex-1-ene 
• 1352632-22-4 C₂₁H₂₀ClNO 

Relevant articles and documents

Studies on the Wittig reaction (XXX): Stereoselective synthesis and bioactivity of 1-aryl-6-(1,2,4-triazol-1-yl)-1-hexenes

Twelve 1-aryl-6-(1,2,4-triazol-1-yl)-1-hexenes 4 were synthesized by N-alkylation of alkenyl bromides 3, which were obtained by the Wittig reaction of 5-hydroxypentyltriphenylphosphonium bromide 1 with various aromatic aldehydes and subsequent bromination

One-pot synthesis of benzo[f]quinolin-3-ones and benzo[a]phenanthridein-5- ones by the photoanuulation of 6-chloropyridin-2-ones and 3-chloroisoquinolin-1- ones to phenylacetylene

The one-pot synthesis of benzo[f]quinolin-3-ones and benzo[a] phenanthridein-5-ones was achieved by the inter- and intramolecular photoannulation of 6-chloropyridin-2-ones and 3-chloroisoquinolin-1-ones with phenylacetylene or tethered phenylacetylene. The reactions were proceeded by photoaddition of 6-chloropyridin-2-ones and 3-chloroisoquinolin-1-ones to phenylacetylene to give the chlorine-substituted stilbenoids, and then 6π electrocyclization of the stilbenoids and oxidation aromatization to afford the polycyclic products.