Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

(3-Benzyloxypropyl)triphenylphosphonium bromide

Base Information
  • Chemical Name:(3-Benzyloxypropyl)triphenylphosphonium bromide
  • CAS No.:54314-85-1
  • Molecular Formula:C28H28 O P . Br
  • Molecular Weight:491.407
  • Hs Code.:2931900090
  • European Community (EC) Number:628-720-6
  • DSSTox Substance ID:DTXSID90448639
  • Mol file:54314-85-1.mol
(3-Benzyloxypropyl)triphenylphosphonium bromide

Synonyms:54314-85-1;(3-Benzyloxypropyl)triphenylphosphonium bromide;[3-(Benzyloxy)propyl]triphenylphosphonium Bromide;triphenyl(3-phenylmethoxypropyl)phosphanium;bromide;MFCD00191781;Phosphonium, triphenyl[3-(phenylmethoxy)propyl]-, bromide;3-Benzyloxypropyl(triphenyl)phosphonium bromide;(3-(benzyloxy)propyl)triphenylphosphonium bromide;(3-Benzyloxypropyl)triphenylphosphoniumbromide;[3-(Benzyloxy)propyl]triphenylphosphoniumBromide;SCHEMBL79890;DTXSID90448639;DWYCJWXMZGVGJV-UHFFFAOYSA-M;AKOS015913243;AB87253;PS-19293;SY024113;3-Benzyloxypropyltriphenylphosphonium Bromide;CS-0183227;FT-0640237;3-benzyloxypropyl(triphenyl)phosphonium;(3-benzyloxypropyl)triphenyl phosphonium bromide;(3-benzyloxypropyl)triphenyl-phosphonium bromide;[3-(Benzyloxy)propyl](triphenyl)phosphanium bromide;triphenyl{3-[(phenylmethyl)oxy]propyl}phosphonium bromide

Suppliers and Price of (3-Benzyloxypropyl)triphenylphosphonium bromide
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
  • TRC
  • (3-Benzyloxypropyl)triphenylphosphonium bromide
  • 1g
  • $ 160.00
  • TRC
  • (3-Benzyloxypropyl)triphenylphosphonium bromide
  • 10g
  • $ 1260.00
  • Sigma-Aldrich
  • (3-Benzyloxypropyl)triphenylphosphonium bromide 98%
  • 5g
  • $ 164.00
  • Crysdot
  • (3-Benzyloxypropyl)triphenylphosphonium bromide 95+%
  • 25g
  • $ 428.00
  • American Custom Chemicals Corporation
  • (3-BENZYLOXYPROPYL)TRIPHENYLPHOSPHONIUM BROMIDE 95.00%
  • 5G
  • $ 933.21
  • Alichem
  • (3-Benzyloxypropyl)triphenylphosphonium bromide
  • 5g
  • $ 387.84
  • Alichem
  • (3-Benzyloxypropyl)triphenylphosphonium bromide
  • 25g
  • $ 432.28
  • Alfa Aesar
  • (3-Benzyloxypropyl)triphenylphosphonium bromide, 97+%
  • 25g
  • $ 504.00
  • Alfa Aesar
  • (3-Benzyloxypropyl)triphenylphosphonium bromide, 97+%
  • 5g
  • $ 130.00
  • Alfa Aesar
  • (3-Benzyloxypropyl)triphenylphosphonium bromide, 97+%
  • 1g
  • $ 35.30
Total 29 raw suppliers
Chemical Property of (3-Benzyloxypropyl)triphenylphosphonium bromide
Chemical Property:
  • Melting Point:153-154 °C(lit.)
     
  • PSA:22.82000 
  • LogP:2.59140 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:9
  • Exact Mass:490.10612
  • Heavy Atom Count:31
  • Complexity:408
Purity/Quality:

97% *data from raw suppliers

(3-Benzyloxypropyl)triphenylphosphonium bromide *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)COCCC[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Br-]
  • Uses Reactant for preparation of:Spirocyclohexadienones via Pd-catalyzed intramolecular ipso-Friedel-Crafts allylic alkylationInhibitors of heat shock protein (Hsp90) as antitumor agentsCarpanone-like molecules via an oxidative coupling/Diels-Alder cycloaddition sequence (3-Benzyloxypropyl)triphenylphosphonium Bromide is a reagent used in the preparation of antitumor and Her2 degradation activity of geldanamycin and radicicol macrocyclic chimeras.
Technology Process of (3-Benzyloxypropyl)triphenylphosphonium bromide

There total 3 articles about (3-Benzyloxypropyl)triphenylphosphonium bromide 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:
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) methanesulfonyl chloride, triethylamine; 2.) lithium bromide / 1.) 30 min, 0 degC, CH2Cl2; 2.) acetone, 6 h, reflux
2: 85 percent / toluene / 7 h / Heating
With methanesulfonyl chloride; triethylamine; lithium bromide; In toluene;
DOI:10.1021/ja00295a027
Guidance literature:
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 54314-85-1