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N-BOC-5-CHLOROTRYPTOPHOL

Base Information Edit
  • Chemical Name:N-BOC-5-CHLOROTRYPTOPHOL
  • CAS No.:898746-66-2
  • Molecular Formula:C15H18ClNO3
  • Molecular Weight:295.766
  • Hs Code.:
  • Mol file:898746-66-2.mol
N-BOC-5-CHLOROTRYPTOPHOL

Synonyms:N-BOC-5-CHLOROTRYPTOPHOL

Suppliers and Price of N-BOC-5-CHLOROTRYPTOPHOL
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
  • American Custom Chemicals Corporation
  • N-BOC-5-CHLOROTRYPTOPHOL 95.00%
  • 5G
  • $ 1249.13
  • American Custom Chemicals Corporation
  • N-BOC-5-CHLOROTRYPTOPHOL 95.00%
  • 100MG
  • $ 420.00
Total 4 raw suppliers
Chemical Property of N-BOC-5-CHLOROTRYPTOPHOL Edit
Chemical Property:
  • PSA:51.46000 
  • LogP:3.61270 
Purity/Quality:

97% *data from raw suppliers

N-BOC-5-CHLOROTRYPTOPHOL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of N-BOC-5-CHLOROTRYPTOPHOL

There total 3 articles about N-BOC-5-CHLOROTRYPTOPHOL 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 tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 - 20 ℃; for 5h;
DOI:10.1055/a-1310-5213
Guidance literature:
Multi-step reaction with 2 steps
1: dmap / dichloromethane / 2 h / 20 °C
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 5 h / 0 - 20 °C
With dmap; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane;
DOI:10.1055/a-1310-5213
Guidance literature:
Multi-step reaction with 3 steps
1: 1H-imidazole / N,N-dimethyl-formamide / 4.5 h / 0 - 20 °C
2: dmap / dichloromethane / 2 h / 20 °C
3: tetrabutyl ammonium fluoride / tetrahydrofuran / 5 h / 0 - 20 °C
With 1H-imidazole; dmap; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1055/a-1310-5213
upstream raw materials:

2-(5-chloro-1H-indol-3-yl)ethanol

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