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methyl naphthalen-1-ylcarbamate

Base Information Edit
  • Chemical Name:methyl naphthalen-1-ylcarbamate
  • CAS No.:5449-00-3
  • Molecular Formula:C12H11NO2
  • Molecular Weight:201.225
  • Hs Code.:
  • Mol file:5449-00-3.mol
methyl naphthalen-1-ylcarbamate

Synonyms:

Suppliers and Price of methyl naphthalen-1-ylcarbamate
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
Total 3 raw suppliers
Chemical Property of methyl naphthalen-1-ylcarbamate Edit
Chemical Property:
  • Vapor Pressure:0.00106mmHg at 25°C 
  • Boiling Point:301.4°Cat760mmHg 
  • Flash Point:136.1°C 
  • Density:1.234g/cm3 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of methyl naphthalen-1-ylcarbamate

There total 1 articles about methyl naphthalen-1-ylcarbamate 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 [2,2]bipyridinyl; dodecacarbonyl-triangulo-triruthenium; montmorillonitebipyridynylpalladium(II) acetate (Pd-clay); In benzene; at 180 ℃; for 24h; under 53200 Torr;
DOI:10.1021/ja00062a055
Guidance literature:
With silver hexafluoroantimonate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; oxygen; copper(II) acetate monohydrate; In 1,2-dichloro-ethane; at 100 ℃; for 12h;
DOI:10.1021/ol502317c
Guidance literature:
With 2-chloro-1,3,2-benzodioxaborole; triethylamine; In toluene; 1.) reflux, 5 min, 2.) 0.5 h;
DOI:10.1021/jo00106a044
Refernces Edit
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