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tert-Butyl formylcarbamate

Base Information
  • Chemical Name:tert-Butyl formylcarbamate
  • CAS No.:913344-40-8
  • Molecular Formula:C6H11NO3
  • Molecular Weight:145.158
  • Hs Code.:
tert-Butyl formylcarbamate

Synonyms:tert-Butyl formylcarbamate

Suppliers and Price of tert-Butyl formylcarbamate
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
  • Crysdot
  • tert-Butylformylcarbamate 95+%
  • 5g
  • $ 594.00
Total 6 raw suppliers
Chemical Property of tert-Butyl formylcarbamate
Chemical Property:
  • PSA:58.89000 
  • Density:1.057±0.06 g/cm3(Predicted) 
  • LogP:1.50780 
Purity/Quality:

98% *data from raw suppliers

tert-Butylformylcarbamate 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of tert-Butyl formylcarbamate

There total 2 articles about tert-Butyl formylcarbamate 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 periodate; In water; at 20 ℃; for 1h; Darkness;
DOI:10.1002/anie.202109769
Guidance literature:
With N-hydroxyphthalimide; oxygen; cobalt(II) acetate; In acetonitrile; at 25 ℃; for 24h; Kinetics;
DOI:10.1016/j.tet.2019.05.026
Guidance literature:
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine; triethylamine; (S)-(+)-(3,5-dioxa-4-phosphacyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)-bis-[(1S)-1-(2-methoxy-phenyl)ethyl]amine; In tetrahydrofuran; at 20 ℃; for 48h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1055/s-0028-1083158
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