N-Acetyl-5-benzyloxy-DL-tryptophan

Base Information

Chemical Name:N-Acetyl-5-benzyloxy-DL-tryptophan
CAS No.:55443-80-6
Molecular Formula:C₂₀H₂₀N₂O₄
Molecular Weight:352.39
Hs Code.:
DSSTox Substance ID:DTXSID20370631
Mol file:55443-80-6.mol

Synonyms:N-Acetyl-5-benzyloxy-DL-tryptophan;55443-80-6;2-acetamido-3-(5-phenylmethoxy-1H-indol-3-yl)propanoic Acid;53017-51-9;2-Acetamido-3-(5-(benzyloxy)-1H-indol-3-yl)propanoic acid;SCHEMBL11682927;DTXSID20370631;3-[5-(benzyloxy)-1H-indol-3-yl]-2-acetamidopropanoic acid;AKOS027383173;FT-0629799;A-0540;2-Acetamido-3-(5-(benzyloxy)-1H-indol-3-yl)propanoicacid

Suppliers and Price of N-Acetyl-5-benzyloxy-DL-tryptophan

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-ACETYL-5-BENZYLOXY-DL-TRYPTOPHAN 95.00%
1G
$ 1155.00

American Custom Chemicals Corporation
N-ACETYL-5-BENZYLOXY-DL-TRYPTOPHAN 95.00%
500MG
$ 1001.66

AHH
DL-N-Acetyl-2-amino-3-(5-benzyloxyindolyl)propionicacid 97%
1g
$ 328.00

Total 7 raw suppliers

Chemical Property of N-Acetyl-5-benzyloxy-DL-tryptophan

Chemical Property:

Vapor Pressure:3.62E-19mmHg at 25°C
Refractive Index:1.648
Boiling Point:675.5°C at 760 mmHg
Flash Point:362.3°C
PSA：91.42000
Density:1.305g/cm³
LogP:3.26960
XLogP3:2.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:352.14230712
Heavy Atom Count:26
Complexity:492

Purity/Quality:

98%min ^*data from raw suppliers

N-ACETYL-5-BENZYLOXY-DL-TRYPTOPHAN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC(CC1=CNC2=C1C=C(C=C2)OCC3=CC=CC=C3)C(=O)O

Technology Process of N-Acetyl-5-benzyloxy-DL-tryptophan

There total 5 articles about N-Acetyl-5-benzyloxy-DL-tryptophan 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: 82.0%

: 53017-44-0,93380-57-5
5-benzyloxy-N_b-acetyl-L-tryptophan methyl ester

: 53017-51-9,55443-80-6,56777-73-2,56777-74-3
5-benzyloxy-N_b-acetyl-L-tryptophan

Guidance literature:: With sodium hydroxide; In methanol; for 2h; Ambient temperature;

Reference yield:

: 2311-25-3,18800-83-4,27460-51-1,114376-47-5
N-acetyl-L-proline methyl ester

: 53017-51-9,55443-80-6,56777-73-2,56777-74-3
5-benzyloxy-N_b-acetyl-L-tryptophan

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / Et₄NClO₄ / acetonitrile / Ambient temperature; anodic oxidation with Pt electrodes

2: 79 percent / AcOH / H₂O / 2 h / 80 - 90 °C

3: 82 percent / 1 N NaOH / methanol / 2 h / Ambient temperature

With sodium hydroxide; tetraethylammonium perchlorate; acetic acid; In methanol; water; acetonitrile;

Reference yield:

: 154005-67-1
(S)-1-Acetyl-5-hydroxy-pyrrolidine-2-carboxylic acid methyl ester

: 53017-51-9,55443-80-6,56777-73-2,56777-74-3
5-benzyloxy-N_b-acetyl-L-tryptophan

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / AcOH / H₂O / 2 h / 80 - 90 °C

2: 82 percent / 1 N NaOH / methanol / 2 h / Ambient temperature

With sodium hydroxide; acetic acid; In methanol; water;