Indoleacetyl glutamic acid

Base Information

Chemical Name:Indoleacetyl glutamic acid
CAS No.:57105-48-3
Molecular Formula:C15H16N2O5
Molecular Weight:304.29800
Hs Code.:
UNII:WG2R895X5T
DSSTox Substance ID:DTXSID70205727
Nikkaji Number:J1.110.325A
Wikidata:Q27292619

Synonyms:Indoleacetyl glutamic acid;57105-48-3;Auxistim G;Indole-3-acetylglutamic acid;Indole-3-acetyl glutamate;N-(3-indolylacetyl)-L-glutamic acid;UNII-WG2R895X5T;Glutamic acid, N-(indol-3-ylacetyl)-;WG2R895X5T;L-Glutamic acid, N-(2-(1H-indol-3-yl)acetyl)-;(2S)-2-[[2-(1H-indol-3-yl)acetyl]amino]pentanedioic Acid;N-(1H-Indol-3-ylacetyl)-L-glutamic acid;(2-(1H-indol-3-yl)acetyl)-L-glutamic acid;Indole-3-acetyl-L-glutamic acid;L-N-(1H-Indol-3-ylacetyl)glutamic acid;SCHEMBL17848778;DTXSID70205727;CHEBI:190884;STL565672;AKOS030601530;N-(indole-3-yl-acetyl)-glutamic acid;N-(1H-Indol-3-ylacetyl)glutamic acid;INDOLEACETYL GLUTAMIC ACID [INCI];S-N-(1H-Indol-3-ylacetyl)glutamic acid;D87701;Q27292619

Suppliers and Price of Indoleacetyl glutamic acid

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

Usbiological
Indole-3-acetyl-L-glutamic Acid
1mg
$ 319.00

TRC
Indole-3-acetyl-L-glutamicAcid
1mg
$ 65.00

Labseeker
N-(3-indolylacetyl)-L-glutamicacid 97
1g
$ 500.00

AK Scientific
2-(2-(1H-Indol-3-yl)acetamido)pentanedioicacid
10g
$ 774.00

Total 6 raw suppliers

Chemical Property of Indoleacetyl glutamic acid

Chemical Property:

Melting Point:167-172°C
PSA：119.49000
LogP:1.53550
Storage Temp.:-20°C Freezer
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:0.6
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:7
Exact Mass:304.10592162
Heavy Atom Count:22
Complexity:440

Purity/Quality:

98% ^*data from raw suppliers

Indole-3-acetyl-L-glutamic Acid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=CN2)CC(=O)NC(CCC(=O)O)C(=O)O
Isomeric SMILES:C1=CC=C2C(=C1)C(=CN2)CC(=O)N[C@@H](CCC(=O)O)C(=O)O
Uses Indole-3-acetyl-L-glutamic Acid 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 Indoleacetyl glutamic acid

There total 6 articles about Indoleacetyl glutamic acid 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: 96.0%

: dimethyl (2S)-2-[(1H-indol-3-ylacetyl)amino]pentanedioate

: 57105-48-3,192430-60-7
N-(indol-3-ylacetyl)-L-glutamic acid

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

Reference yield: 47.0%

: 617-65-2,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6
Glutamic acid

: 145232-25-3
N-(indol-3-ylacetoxy)succinimide

: 57105-48-3,192430-60-7
indole-3-acetyl-N-glutamic acid

Guidance literature:: With sodium hydrogencarbonate; In 1,4-dioxane; Ambient temperature;
DOI:10.1002/(SICI)1099-1344(199705)39:5<433::AID-JLCR987>3.0.CO;2-H

Reference yield:

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

: 23150-65-4
L-glutamic dimethyl ester hydrochloride

: 57105-48-3,192430-60-7
N-(indol-3-ylacetyl)-L-glutamic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; benzotriazol-1-ol / dichloromethane / 0 - 20 °C

2: sodium hydroxide / methanol / 1.5 h / 20 °C

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In methanol; dichloromethane;
DOI:10.1080/00397911.2019.1605446