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1-(tert-Butoxycarbonyl)-6-methoxyindole

Base Information
  • Chemical Name:1-(tert-Butoxycarbonyl)-6-methoxyindole
  • CAS No.:138344-18-0
  • Molecular Formula:C14H17NO3
  • Molecular Weight:247.294
  • Hs Code.:2933990090
  • Mol file:138344-18-0.mol
1-(tert-Butoxycarbonyl)-6-methoxyindole

Synonyms:tert-Butyl 6-methoxy-1H-indole-1-carboxylate;

Suppliers and Price of 1-(tert-Butoxycarbonyl)-6-methoxyindole
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
  • Chemenu
  • tert-butyl6-methoxy-1H-indole-1-carboxylate 95%
  • 5g
  • $ 297.00
  • Chemcia Scientific
  • 6-Methoxy-indole-1-carboxylicacidtert-butylester 95%
  • 5 G
  • $ 385.00
  • American Custom Chemicals Corporation
  • 1-BOC-6-METHOXYINDOLE 95.00%
  • 5G
  • $ 1370.41
  • American Custom Chemicals Corporation
  • 1-BOC-6-METHOXYINDOLE 95.00%
  • 1G
  • $ 751.91
  • AK Scientific
  • N-Boc-6-methoxyindole
  • 5g
  • $ 584.00
Total 14 raw suppliers
Chemical Property of 1-(tert-Butoxycarbonyl)-6-methoxyindole
Chemical Property:
  • Vapor Pressure:2.75E-05mmHg at 25°C 
  • Refractive Index:1.531 
  • Boiling Point:357.3 °C at 760 mmHg 
  • Flash Point:169.9 °C 
  • PSA:40.46000 
  • Density:1.1 g/cm3 
  • LogP:3.43310 
  • Storage Temp.:2-8°C 
Purity/Quality:

98%min *data from raw suppliers

tert-butyl6-methoxy-1H-indole-1-carboxylate 95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 1-Boc-6-methoxyindole is used as a reactant in the preparation of substituted indoles for treating hepatitis C.
Technology Process of 1-(tert-Butoxycarbonyl)-6-methoxyindole

There total 5 articles about 1-(tert-Butoxycarbonyl)-6-methoxyindole 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 dmap; In dichloromethane; at 20 ℃; for 8h; Inert atmosphere;
DOI:10.1016/j.tet.2009.06.071
Guidance literature:
With hydrogenchloride; In tetrahydrofuran; for 0.0833333h; Yield given; Ambient temperature;
DOI:10.1055/s-1991-26597
Guidance literature:
Multi-step reaction with 3 steps
1: tetrahydrofuran / Heating
2: 1a) s-BuLi, 2) DMF / 1a) THF, cyclohexane, -45 to -55 deg C, 30 min, 1b) -> -15 deg C, 60 min, 2) -45 deg C, 5 min
3: 12N HCl / tetrahydrofuran / 0.08 h / Ambient temperature
With hydrogenchloride; sec.-butyllithium; N,N-dimethyl-formamide; In tetrahydrofuran;
DOI:10.1055/s-1991-26597
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