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Home Bromides 2695-48-9
2695-48-9,MFCD00000275
Catalog No.:AA003NEU

2695-48-9 | 8-Bromo-1-octene

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$11.00   $8.00
- +
5g
98%
in stock  
$14.00   $10.00
- +
25g
95%
in stock  
$56.00   $39.00
- +
100g
98%
in stock  
$144.00   $101.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003NEU
Chemical Name:
8-Bromo-1-octene
CAS Number:
2695-48-9
Molecular Formula:
C8H15Br
Molecular Weight:
191.1087
MDL Number:
MFCD00000275
SMILES:
BrCCCCCCC=C
Properties
Properties
 
BP:
198.7°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.467(lit.)  
Storage:
Inert atmosphere;2-8℃;Light sensitive;  

Computed Properties
 
Complexity:
59.6  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Rotatable Bond Count:
6  
XLogP3:
3.9  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,2001,vol.44,#7,p.1099-1115

[2]TetrahedronLetters,1979,vol.No.50,p.4851-4854

[3]ChemistryofNaturalCompounds,1982,vol.18,#2,p.219-224

[4]KhimiyaPrirodnykhSoedinenii,1982,vol.18,#2,p.239-245

[1]Patent:US5405997,1995,A,

[1]LiebigsAnnalenderChemie,1982,#6,p.1216-1219

[1]JournalofOrganicChemistry,2004,vol.69,#19,p.6185-6201

Downstream Synthesis Route

[1]AngewandteChemie-InternationalEdition,2017,vol.56,p.4342-4346    Angew.Chem.,2017,vol.129,p.4406-4410,5

[2]ChemistryofNaturalCompounds,1982,vol.18,p.219-224    KhimiyaPrirodnykhSoedinenii,1982,vol.18,p.239-245

[3]Patent:WO2015/136093,2015,A1.Locationinpatent:Page/Pagecolumn26

[4]TetrahedronLetters,1979,vol.No.50,p.4851-4854

[5]ChemistryofNaturalCompounds,1992,vol.28,p.369-374    KhimiyaPrirodnykhSoedinenii,1992,p.423-429

[6]Macromolecules,2015,vol.48,p.5470-5473

[1]JournalofMedicinalChemistry,2001,vol.44,p.1099-1115

[2]TetrahedronLetters,1979,vol.No.50,p.4851-4854

[3]ChemistryofNaturalCompounds,1982,vol.18,p.219-224    KhimiyaPrirodnykhSoedinenii,1982,vol.18,p.239-245

[1]JournaloftheAmericanChemicalSociety,2007,vol.129,p.2938-2953

[2]SyntheticCommunications,2001,vol.31,p.1367-1371

[3]BioorganicandMedicinalChemistry,2018,vol.26,p.4047-4057

[4]Chemistry-AEuropeanJournal,2013,vol.19,p.1002-1012

[5]JournalofOrganicChemistry,2001,vol.66,p.4304-4310

[6]TetrahedronLetters,1983,vol.24,p.5305-5308

[7]TetrahedronAsymmetry,2005,vol.16,p.2501-2508

[8]ZeitschriftfurNaturforschung,B:ChemicalSciences,2010,vol.65,p.414-424

486-60-2    2695-48-9   
5-oct-7''-enyloxy-psoralen 

[1]PhotochemistryandPhotobiology,1996,vol.63,p.176-181

40882-83-5    2695-48-9   
5,10,15,20-tetra(N-7-octenylpyridinium-3-yl)porphyrintetrabromide 

[1]Dancil,Keiki-PuaS.;Hilario,LynnF.;Khoury,RichardG.;Mai,KimU.;Nguyen,ChiK.;Weddle,KatherineS.;Shachter,AmyM.[JournalofHeterocyclicChemistry,1997,vol.34,#3,p.749-755]

Literature

Title: Replacing conventional carbon nucleophiles with electrophiles: nickel-catalyzed reductive alkylation of aryl bromides and chlorides.

Journal: Journal of the American Chemical Society 20120411

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