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methyl N-(2-bromo-4-methylphenyl)carbamate

Base Information
  • Chemical Name:methyl N-(2-bromo-4-methylphenyl)carbamate
  • CAS No.:540797-44-2
  • Molecular Formula:C9H10BrNO2
  • Molecular Weight:244.088
  • Hs Code.:
methyl N-(2-bromo-4-methylphenyl)carbamate

Synonyms:methyl N-(2-bromo-4-methylphenyl)carbamate

Suppliers and Price of methyl N-(2-bromo-4-methylphenyl)carbamate
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
  • METHYL N-(2-BROMO-4-METHYLPHENYL)CARBAMATE 95.00%
  • 5G
  • $ 1295.03
  • American Custom Chemicals Corporation
  • METHYL N-(2-BROMO-4-METHYLPHENYL)CARBAMATE 95.00%
  • 2.5G
  • $ 1065.66
  • American Custom Chemicals Corporation
  • METHYL N-(2-BROMO-4-METHYLPHENYL)CARBAMATE 95.00%
  • 1G
  • $ 765.23
  • AK Scientific
  • MethylN-(2-bromo-4-methylphenyl)carbamate
  • 100mg
  • $ 172.00
Total 1 raw suppliers
Chemical Property of methyl N-(2-bromo-4-methylphenyl)carbamate
Chemical Property:
Purity/Quality:

METHYL N-(2-BROMO-4-METHYLPHENYL)CARBAMATE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of methyl N-(2-bromo-4-methylphenyl)carbamate

There total 3 articles about methyl N-(2-bromo-4-methylphenyl)carbamate 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 N-Bromosuccinimide; palladium diacetate; toluene-4-sulfonic acid; In 1,2-dichloro-ethane; at 60 ℃; for 3h; Reagent/catalyst; Temperature; Solvent; regioselective reaction; Catalytic behavior; Sealed tube;
DOI:10.1021/acs.joc.6b00329
Guidance literature:
Multi-step reaction with 2 steps
1: N-Bromosuccinimide; potassium tert-butylate / 0.67 h / 80 °C
2: N-Bromosuccinimide; toluene-4-sulfonic acid; palladium diacetate / 1,2-dichloro-ethane / 3 h / 60 °C / Sealed tube
With N-Bromosuccinimide; potassium tert-butylate; palladium diacetate; toluene-4-sulfonic acid; In 1,2-dichloro-ethane;
DOI:10.1021/acs.joc.6b00329
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