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Bromoclenbuterol

Base Information
  • Chemical Name:Bromoclenbuterol
  • CAS No.:37153-52-9
  • Molecular Formula:C12H18BrClN2O
  • Molecular Weight:321.645
  • Hs Code.:2922199090
  • DSSTox Substance ID:DTXSID80376770
  • Nikkaji Number:J3.169.928B
  • Mol file:37153-52-9.mol
Bromoclenbuterol

Synonyms:Bromoclenbuterol;37153-52-9;1-(4-amino-3-bromo-5-chlorophenyl)-2-(tert-butylamino)ethanol;Clenbuterol Impurity F;Bromchlorbuterol;Chlorbrombuterol;SCHEMBL10614327;DTXSID80376770;FT-0730841

Suppliers and Price of Bromoclenbuterol
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
  • American Custom Chemicals Corporation
  • BROMOCLENBUTEROL 95.00%
  • 5MG
  • $ 499.10
Total 25 raw suppliers
Chemical Property of Bromoclenbuterol
Chemical Property:
  • Vapor Pressure:3.61E-08mmHg at 25°C 
  • Boiling Point:430.3°Cat760mmHg 
  • Flash Point:214°C 
  • PSA:58.28000 
  • Density:1.424g/cm3 
  • LogP:4.07830 
  • XLogP3:2.3
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:320.02910
  • Heavy Atom Count:17
  • Complexity:247
Purity/Quality:

99% *data from raw suppliers

BROMOCLENBUTEROL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)NCC(C1=CC(=C(C(=C1)Br)N)Cl)O
  • Uses Bromoclenbuterol is a β-agonist in human urine.
Technology Process of Bromoclenbuterol

There total 5 articles about Bromoclenbuterol 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:
tert-butylamine; 4-amino-3-bromo-5-chlorobromoacetophenone; In tetrahydrofuran; ethanol; at 0 - 20 ℃; for 4h; Inert atmosphere;
With potassium borohydride; In tetrahydrofuran; ethanol; for 2h; Cooling with ice;
With methanol; In tetrahydrofuran; ethanol;
Guidance literature:
Multi-step reaction with 3 steps
1.1: N-Bromosuccinimide / acetonitrile / 2 h / 20 °C
2.1: copper(ll) bromide / ethyl acetate; chloroform; ethanol / 2 h / Reflux
3.1: ethanol; tetrahydrofuran / 4 h / 0 - 20 °C / Inert atmosphere
3.2: 2 h / Cooling with ice
With N-Bromosuccinimide; copper(ll) bromide; In tetrahydrofuran; ethanol; chloroform; ethyl acetate; acetonitrile;
Guidance literature:
Multi-step reaction with 2 steps
1.1: copper(ll) bromide / ethyl acetate; chloroform; ethanol / 2 h / Reflux
2.1: ethanol; tetrahydrofuran / 4 h / 0 - 20 °C / Inert atmosphere
2.2: 2 h / Cooling with ice
With copper(ll) bromide; In tetrahydrofuran; ethanol; chloroform; ethyl acetate;
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