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3,4,5-Trimethylphenyl bromide

Base Information
  • Chemical Name:3,4,5-Trimethylphenyl bromide
  • CAS No.:32591-43-8
  • Molecular Formula:C9H11Br
  • Molecular Weight:199.09
  • Hs Code.:
  • Mol file:32591-43-8.mol
3,4,5-Trimethylphenyl bromide

Synonyms:5-bromo-1,2,3-trimethyl-benzene;5-Brom-1,2,3-trimethyl-benzol;3,4,5-Trimethyl-brom-benzol;Benzene, 5-bromo-1,2,3-trimethyl;3,4,5-trimethyl-bromobenzene;

Suppliers and Price of 3,4,5-Trimethylphenyl 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
  • Alichem
  • 1-Bromo-3,4,5-trimethylbenzene
  • 1g
  • $ 1519.80
  • Alichem
  • 1-Bromo-3,4,5-trimethylbenzene
  • 500mg
  • $ 782.40
Total 8 raw suppliers
Chemical Property of 3,4,5-Trimethylphenyl bromide
Chemical Property:
  • Melting Point:20℃ 
  • Boiling Point:110-112℃ (12 Torr) 
  • PSA:0.00000 
  • Density:1.289±0.06 g/cm3(Predicted) 
  • LogP:3.37430 
Purity/Quality:

99.3% *data from raw suppliers

1-Bromo-3,4,5-trimethylbenzene *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 3,4,5-Trimethylphenyl bromide

There total 8 articles about 3,4,5-Trimethylphenyl 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:
With hydrogenchloride; bromine; Behandeln des Reaktionsprodukts mit wss. Salzsaeure und Natriumnitrit und anschliessend Behandeln mit Hypophosphorigsaeure;
DOI:10.1021/ja01107a030
Guidance literature:
Multi-step reaction with 5 steps
1: 50 percent / butyllithium in ether / -60 °C
2: 1.) SOCl2; 2.) NaN3 in water, tetrabutylammonium bromide / 1.) methylene dichloride; 2.) 0 deg C, 2 h
3: 1.) trifluoroacetic acid; 2.) K2CO3 / 1.) CHCl2, reflux, 6 h; 2.) aq. methanol, 20 h
4: 75 percent / NBS / dimethylformamide / 24 h
5: 1.) conc. HCl, aq. NaNO2; 2.) 50percent H3PO3 / 1.) acetic anhydride; 2.) 0 deg C, 1 h
With hydrogenchloride; N-Bromosuccinimide; n-butyllithium; phosphonic Acid; thionyl chloride; sodium azide; tetrabutylammomium bromide; potassium carbonate; trifluoroacetic acid; sodium nitrite; In N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) SOCl2; 2.) NaN3 in water, tetrabutylammonium bromide / 1.) methylene dichloride; 2.) 0 deg C, 2 h
2: 1.) trifluoroacetic acid; 2.) K2CO3 / 1.) CHCl2, reflux, 6 h; 2.) aq. methanol, 20 h
3: 75 percent / NBS / dimethylformamide / 24 h
4: 1.) conc. HCl, aq. NaNO2; 2.) 50percent H3PO3 / 1.) acetic anhydride; 2.) 0 deg C, 1 h
With hydrogenchloride; N-Bromosuccinimide; phosphonic Acid; thionyl chloride; sodium azide; tetrabutylammomium bromide; potassium carbonate; trifluoroacetic acid; sodium nitrite; In N,N-dimethyl-formamide;
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