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N-(4-broMobenzyl)-O-MethylhydroxylaMine

Base Information Edit
  • Chemical Name:N-(4-broMobenzyl)-O-MethylhydroxylaMine
  • CAS No.:916582-47-3
  • Molecular Formula:C8H10BrNO
  • Molecular Weight:216.077
  • Hs Code.:
  • Mol file:916582-47-3.mol
N-(4-broMobenzyl)-O-MethylhydroxylaMine

Synonyms:N-(4-broMobenzyl)-O-MethylhydroxylaMine

Suppliers and Price of N-(4-broMobenzyl)-O-MethylhydroxylaMine
Supply Marketing:Edit
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
  • Matrix Scientific
  • N-(4-Bromobenzyl)-O-methylhydroxylamine 95%
  • 1g
  • $ 213.00
  • Matrix Scientific
  • N-(4-Bromobenzyl)-O-methylhydroxylamine 95%
  • 5g
  • $ 657.00
  • A1 Biochem Labs
  • [(4-Bromophenyl)methyl](methoxy)amine 95%
  • 5 g
  • $ 600.00
Total 2 raw suppliers
Chemical Property of N-(4-broMobenzyl)-O-MethylhydroxylaMine Edit
Chemical Property:
  • PSA:21.26000 
  • LogP:2.49100 
Purity/Quality:

99% *data from raw suppliers

N-(4-Bromobenzyl)-O-methylhydroxylamine 95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of N-(4-broMobenzyl)-O-MethylhydroxylaMine

There total 2 articles about N-(4-broMobenzyl)-O-MethylhydroxylaMine 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 sodium cyanoborohydride; acetyl chloride; In methanol; at 0 - 20 ℃; for 1h; Inert atmosphere;
DOI:10.1002/anie.201308905
Guidance literature:
Multi-step reaction with 2 steps
1: pyridine / ethanol / 1 h / 20 °C / Inert atmosphere
2: acetyl chloride; sodium cyanoborohydride / methanol / 1 h / 0 - 20 °C / Inert atmosphere
With pyridine; sodium cyanoborohydride; acetyl chloride; In methanol; ethanol;
DOI:10.1002/anie.201308905
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