N-BOC-4-BROMOTRYPTOPHOL

Base Information

Chemical Name:N-BOC-4-BROMOTRYPTOPHOL
CAS No.:898746-58-2
Molecular Formula:C15H18BrNO3
Molecular Weight:340.21
Hs Code.:
Mol file:898746-58-2.mol

Synonyms:N-BOC-4-BROMOTRYPTOPHOL

Suppliers and Price of N-BOC-4-BROMOTRYPTOPHOL

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
N-BOC-4-BROMOTRYPTOPHOL 95.00%
5G
$ 1249.13

Total 4 raw suppliers

Chemical Property of N-BOC-4-BROMOTRYPTOPHOL

Chemical Property:

PSA：51.46000
LogP:3.72180

Purity/Quality:

95% ^*data from raw suppliers

N-BOC-4-BROMOTRYPTOPHOL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-BOC-4-BROMOTRYPTOPHOL

There total 3 articles about N-BOC-4-BROMOTRYPTOPHOL 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:

Reference yield:

: 1580470-95-6
C₂₁H₃₂BrNO₃Si

: 898746-58-2
tert-butyl 4-bromo-3-(2-hydroxyethyl)-1H-indole-1-carboxylate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1021/ol5004109

Reference yield:

: 202753-56-8
2-(1H-4-bromoindol-3-yl)-ethanol

: 898746-58-2
tert-butyl 4-bromo-3-(2-hydroxyethyl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 1H-imidazole / N,N-dimethyl-formamide / 0 - 20 °C / Inert atmosphere

2: dmap / dichloromethane / 2 h / 20 °C / Inert atmosphere

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 - 20 °C

With 1H-imidazole; dmap; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol5004109

Reference yield:

: 1355951-82-4
C₁₆H₂₄BrNOSi

: 898746-58-2
tert-butyl 4-bromo-3-(2-hydroxyethyl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: dmap / dichloromethane / 2 h / 20 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 - 20 °C

With dmap; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ol5004109