N-(3-Indolylacetyl)-L-phenylalanine

Base Information

• Chemical Name: N-(3-Indolylacetyl)-L-phenylalanine
• CAS No.: 57105-50-7
• Molecular Formula: C₁₉H₁₈N₂O₃
• Molecular Weight: 322.364
• Hs Code.: 2933990090
• Mol file: 57105-50-7.mol

Synonyms:L-Phenylalanine,N-(1H-indol-3-ylacetyl)- (9CI); Indole-3-acetylphenylalanine;N-(3-Indolylacetyl)-L-phenylalanine

Chemical Property of N-(3-Indolylacetyl)-L-phenylalanine

Chemical Property:

• Vapor Pressure: 2.94E-18mmHg at 25°C
• Melting Point: 154-156 ºC
• Boiling Point: 658.9 °C at 760 mmHg
• Flash Point: 352.3 °C
• PSA: 82.19000
• Density: 1.311 g/cm³
• LogP: 2.91340
• Storage Temp.: -20°C

Purity/Quality:

97% ^*data from raw suppliers

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

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 25
• Safety Statements: 45

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Indole-3-acetyl-L-phenylalanine is an indole-3-acetyl-amino acid conjugate involved in regulatory mechanisms for the control of auxin activity during physiological and pathophysiological responses.

Technology Process of N-(3-Indolylacetyl)-L-phenylalanine

There total 7 articles about N-(3-Indolylacetyl)-L-phenylalanine 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)-2-[(1H-indol-3-ylacetyl)amino]-3-phenylpropanoate → (2S)-2-[(1H-indol-3-ylacetyl)amino]-3-phenylpropanoic acid (57105-50-7)

Guidance literature:

With sodium hydroxide; In methanol; at 20 ℃; for 1.5h;

DOI:10.1080/00397911.2019.1605446

Reference yield: 70.0%

1-(1H-benzotriazol-1-yl)-2-(1H-indol-3-yl)ethanone (1080025-88-2) + Phenylalanine (150-30-1,25191-15-5,658-69-5,67675-33-6) → 2-(2-(1H-indol-3-yl)acetamido)-3-phenylpropanoic acid (92519-27-2,57105-50-7)

Guidance literature:

1-(1H-benzotriazol-1-yl)-2-(1H-indol-3-yl)ethanone; Phenylalanine; With triethylamine; In water; acetonitrile; at 20 ℃; for 1h;

With hydrogenchloride; In water; acetonitrile;

DOI:10.1021/jo8017796

Reference yield: 66.0%

1-(1H-benzotriazol-1-yl)-2-(1H-indol-3-yl)ethanone (1080025-88-2) + L-phenylalanine (63-91-2,25191-15-5,658-69-5,67675-33-6) → (2S)-2-[(1H-indol-3-ylacetyl)amino]-3-phenylpropanoic acid (57105-50-7)

Guidance literature:

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

With hydrogenchloride; In water; acetonitrile;

DOI:10.1021/jo8017796

upstream raw materials:

1-(1H-benzotriazol-1-yl)-2-(1H-indol-3-yl)ethanone

Phenylalanine

L-phenylalanine

indole-3-acetic acid

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