Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Carbamic acid, [(1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethyl]-, phenylmethyl ester

Base Information Edit
  • Chemical Name:Carbamic acid, [(1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethyl]-, phenylmethyl ester
  • CAS No.:168110-39-2
  • Molecular Formula:C19H19N3O3
  • Molecular Weight:337.378
  • Hs Code.:
  • Mol file:168110-39-2.mol
Carbamic acid, [(1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethyl]-,
phenylmethyl ester

Synonyms:

Suppliers and Price of Carbamic acid, [(1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethyl]-, phenylmethyl ester
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 1 raw suppliers
Chemical Property of Carbamic acid, [(1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethyl]-, phenylmethyl ester Edit
Chemical Property:
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of Carbamic acid, [(1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethyl]-, phenylmethyl ester

There total 1 articles about Carbamic acid, [(1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethyl]-, phenylmethyl ester 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 4-methyl-morpholine; isobutyl chloroformate; In 1,2-dimethoxyethane;
DOI:10.1021/jm020985q
Guidance literature:
Multi-step reaction with 5 steps
1: pyridine; trichlorophosphate / 1 h / 0 °C / Inert atmosphere
2: palladium 10% on activated carbon; hydrogen / 1,4-dioxane / 24 h / 20 °C
3: trifluoroacetic acid / dichloromethane / 1.5 h / 0 °C / Molecular sieve; Inert atmosphere
4: acetic acid; sodium cyanoborohydride / methanol / 60 h / 20 °C / Inert atmosphere
5: potassium carbonate / methanol / 0.5 h / 0 °C
With pyridine; palladium 10% on activated carbon; hydrogen; sodium cyanoborohydride; potassium carbonate; acetic acid; trifluoroacetic acid; trichlorophosphate; In 1,4-dioxane; methanol; dichloromethane; 3: |Pictet-Spengler Synthesis;
DOI:10.1002/anie.202005748
upstream raw materials:

N-(benzyloxycarbonyl)-D-tryptophan

Downstream raw materials:

strictosidine

Post RFQ for Price