D-Tryptophan, N-acetyl-, ethyl ester

Base Information

Chemical Name:D-Tryptophan, N-acetyl-, ethyl ester
CAS No.:92520-19-9
Molecular Formula:C15H18N2O3
Molecular Weight:274.32
Hs Code.:

Synonyms:2-Acetylamino-3-(1H-indol-3-yl)-propionic acid ethyl ester;

Suppliers and Price of D-Tryptophan, N-acetyl-, ethyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of D-Tryptophan, N-acetyl-, ethyl ester

Chemical Property:

Boiling Point:517.6±40.0 °C(Predicted)
PSA：71.19000
Density:1.208±0.06 g/cm3(Predicted)
LogP:2.16910

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of D-Tryptophan, N-acetyl-, ethyl ester

There total 2 articles about D-Tryptophan, N-acetyl-, ethyl 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:

Reference yield: 40.0%

: 42717-06-6
acetyltryptophan ethylester

: 1218-34-4
N-AcTrp

: 2280-01-5
N-acetyl-D-tryptophan

: 92520-19-9
N-acetyl-D-tryptophan ethyl ester

Guidance literature:: With water; In ethanol; at 25 ℃; for 24h; optical yield given as %ee; enantioselective reaction; Microbiological reaction;
DOI:10.1016/j.tetasy.2010.02.011

Reference yield:

: 64-17-5
ethanol

: 42717-06-6
acetyltryptophan ethylester

: 2382-80-1
N-acetyl-L-tryptophane ethyl ester

: 92520-19-9
N-acetyl-D-tryptophan ethyl ester

Guidance literature:: acetyltryptophan ethylester; With water; In ethanol; at 25 ℃; for 24h; Microbiological reaction;

ethanol; With thionyl chloride; optical yield given as %ee; enantioselective reaction; Reflux;
DOI:10.1016/j.tetasy.2010.02.011