42843-49-2

Basic information

• Product Name: 1-Octene, 1-bromo-, (Z)-
• Synonyms: 1c-bromo-oct-1-ene;(Z)-1-bromo-1-octene;(Z)-1-bromooctene;(Z)-1-bromooct-1-ene
• CAS NO: 42843-49-2
• Molecular Formula: C8H15Br
• Molecular Weight: 191.111
• Mol File: 42843-49-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 183.83°C (estimate)
• Density: 1.1342 (estimate)
• Refractive Index: 1.4590
• CAS DataBase Reference: 1-Octene, 1-bromo-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Octene, 1-bromo-, (Z)-(42843-49-2)
• EPA Substance Registry System: 1-Octene, 1-bromo-, (Z)-(42843-49-2)

Safety Data

• Hazardous Substances Data: 42843-49-2(Hazardous Substances Data)

Upstream product

• 152212-49-2 1,2-dibromooctane 
• 109-73-9 N-butylamine 
• 21948-46-9 1,2-dichlorooctane 

Downstream Products

• 629-05-0 n-octyne 
• 834899-01-3 1r-Hydroxy-2t--cyclopentan 
• 1461-23-0 tributyltin bromide 
• 122184-69-4 exo-cis-2-(1-octenyl)-3-vinylnorbornane 
• 75717-41-8 (Z)-oct-1-enylsulfanyl-benzene 
• 75717-40-7 (E)-oct-1-enylsulfanyl-benzene 
• 50284-91-8 ((1Z,3Z)-Octa-1,3-dienyl)-cyclohexane 
• 110897-20-6 ((1Z,3Z)-Deca-1,3-dienyl)-cyclohexane 
• 63922-86-1 2-hexyl-1-phenyl-3-buten-1-ol 
• 111-66-0 oct-1-ene 
• 51447-08-6 (1,3Z,5E)-undeca-1,3,5-triene 
• 20810-21-3 4-undecene 
• 1239384-09-8 3,3-dimethyl-1,1-diisopropyl-1,3-dihydrobenzo[c][1,2]oxasilole 
• 78645-74-6 (E)-2-Methyl-dec-3-ene 

Relevant articles and documents

DIOLS AS EFFECTIVE COCATALYSTS IN THE PHASE TRANSFER CATALYZED PREPARATION OF 1-ALKYNES FROM 1,2-DIHALIDES

Bis-tertiary diols accelerate bis-eliminations of HX from 1,2-dihalides in the presence of an onium salt as phase transfer catalyst and potassium hydroxyde as base.PEG 400 catalyzes the same elimination, but isomerizations from 1-alkyne to mixtures with the 2-alkyne and the 1,2-diene occur easily.

POLY(STYRYLMETHYLTHIOL) AS AN EFFICIENT DEBROMINATING REAGENT OF 1,2-DIBROMIDES

Dibromides are readily debrominated by means of poly(styrylmethyl thiolate) with formation of the respective olefins.The polymeric reagent with a high content of sulphhydryl groups can be easily prepared from chloromethylated polystyrene; it extends possibilities of protection-deprotection reactions of the double bond.