Tryptophan, N-indol-3-ylacetyl- (6CI)

Base Information

Chemical Name:Tryptophan, N-indol-3-ylacetyl- (6CI)
CAS No.:57105-53-0
Molecular Formula:C21H19 N3 O3
Molecular Weight:361.39
Hs Code.:

Synonyms:L-Tryptophan,N-(1H-indol-3-ylacetyl)- (9CI); Tryptophan, N-indol-3-ylacetyl- (6CI)

Suppliers and Price of Tryptophan, N-indol-3-ylacetyl- (6CI)

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

TRC
Indole-3-acetyl-L-tryptophan
100mg
$ 495.00

TRC
Indole-3-acetyl-L-tryptophan
10mg
$ 85.00

Total 6 raw suppliers

Chemical Property of Tryptophan, N-indol-3-ylacetyl- (6CI)

Chemical Property:

Vapor Pressure:9.31E-25mmHg at 25°C
Melting Point:181-183 °C
Boiling Point:767.2°Cat760mmHg
PKA:3?+-.0.10(Predicted)
Flash Point:417.8°C
PSA：101.47000
Density:1.399g/cm³
LogP:3.84410

Purity/Quality:

98% ^*data from raw suppliers

Indole-3-acetyl-L-tryptophan ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Indole-3-acetyl-L-tryptophan is an indole-3-acetyl-amino acid conjugate involved in regulatory mechanisms for the control of auxin activity during physiological and pathophysiological responses. It may also be used in the synthesis of β-D-galactosidase and β-D-glucosidase inhibitors.

Technology Process of Tryptophan, N-indol-3-ylacetyl- (6CI)

There total 6 articles about Tryptophan, N-indol-3-ylacetyl- (6CI) 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: 95.0%

: methyl (2S)-3-(1H-indol-3-yl)-2-[(1H-indol-3-ylacetyl)amino]propanoate

: 57105-53-0
(2S)-3-(1H-indol-3-yl)-2-[(1H-indol-3-ylacetyl)amino]propanoic acid

Guidance literature:: With sodium hydroxide; In methanol; at 20 ℃; for 1.5h;
DOI:10.1080/00397911.2019.1605446

Reference yield: 45.0%

: 1080025-88-2
1-(1H-benzotriazol-1-yl)-2-(1H-indol-3-yl)ethanone

: 73-22-3,27732-43-0,80206-30-0,27813-82-7
L-Tryptophan

: 57105-53-0
(2S)-3-(1H-indol-3-yl)-2-[(1H-indol-3-ylacetyl)amino]propanoic acid

Guidance literature:: 1-(1H-benzotriazol-1-yl)-2-(1H-indol-3-yl)ethanone; L-Tryptophan; With triethylamine; In water; acetonitrile; at 20 ℃; for 1h;

With hydrogenchloride; In water; acetonitrile;
DOI:10.1021/jo8017796

Reference yield:

: 87-51-4
indole-3-acetic acid

: 7524-52-9,26988-71-6,5619-09-0,14907-27-8,41222-70-2,67557-19-1,109492-62-8
(S)-tryptophan methyl ester hydrochloride

: 57105-53-0
(2S)-3-(1H-indol-3-yl)-2-[(1H-indol-3-ylacetyl)amino]propanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1,1'-carbonyldiimidazole / N,N-dimethyl-formamide / 0.25 h / Inert atmosphere

1.2: Inert atmosphere

2.1: sodium hydroxide

With 1,1'-carbonyldiimidazole; sodium hydroxide; In N,N-dimethyl-formamide;
DOI:10.1007/s00044-014-1314-4