8-Bromo-1-phenyloctan-3-one

Base Information

Chemical Name:8-Bromo-1-phenyloctan-3-one
CAS No.:88068-12-6
Molecular Formula:C₁₄H₁₉BrO
Molecular Weight:283.208
Hs Code.:
DSSTox Substance ID:DTXSID10521074
Wikidata:Q82385339

Synonyms:8-bromo-1-phenyloctan-3-one;8-bromo-1-phenyl-3-octanone;88068-12-6;DTXSID10521074

Suppliers and Price of 8-Bromo-1-phenyloctan-3-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 8-Bromo-1-phenyloctan-3-one

Chemical Property:

PSA：17.07000
LogP:4.14360
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:8
Exact Mass:282.06193
Heavy Atom Count:16
Complexity:185

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CCC(=O)CCCCCBr

Technology Process of 8-Bromo-1-phenyloctan-3-one

There total 4 articles about 8-Bromo-1-phenyloctan-3-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 8-hydroxy-1-phenyloctan-3-one

: 88068-12-6
8-bromo-1-phenyloctan-3-one

Guidance literature:: With 1H-imidazole; bromotriphenylphosphonium bromide; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ja306323x

Reference yield:

: 3277-89-2
phenethylmagnesium bromide

: 4224-70-8
6-bromohexanoic acid

: 88068-12-6
8-bromo-1-phenyloctan-3-one

Guidance literature:: With 1-chloro-1-(dimethylamino)-2-methyl-1-propene; copper(l) iodide; Yield given. Multistep reaction; 1.) THF, dichloromethane, 0 deg C, 3 h; 2.) 0 deg C, 1 h;
DOI:10.1246/cl.1983.1791

Reference yield:

: 502-44-3,24980-41-4,80137-66-2
hexahydro-2H-oxepin-2-one

: 88068-12-6
8-bromo-1-phenyloctan-3-one

Guidance literature:: Multi-step reaction with 3 steps

1: isopropylmagnesium chloride / tetrahydrofuran; diethyl ether / 0 - 20 °C / Inert atmosphere

2: tetrahydrofuran; diethyl ether / 2 h / 0 °C / Inert atmosphere

3: bromotriphenylphosphonium bromide; 1H-imidazole / dichloromethane / 0 - 20 °C / Inert atmosphere

With 1H-imidazole; isopropylmagnesium chloride; bromotriphenylphosphonium bromide; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/ja306323x