Indol-1-yl-acetic acid ethyl ester

Base Information

Chemical Name:Indol-1-yl-acetic acid ethyl ester
CAS No.:61155-69-9
Molecular Formula:C12H13NO2
Molecular Weight:203.241
Hs Code.:
DSSTox Substance ID:DTXSID20359522
Nikkaji Number:J397.679C
Wikidata:Q82140766

Synonyms:61155-69-9;ethyl 2-(1h-indol-1-yl)acetate;indol-1-yl-acetic acid ethyl ester;Ethyl 2-indol-1-ylacetate;SCHEMBL3864912;DTXSID20359522;indole-N-acetic Acid Ethyl Ester;DKMSTBXXTNPNPU-UHFFFAOYSA-N;indole-N-acetic acid, ethyl ester;AKOS008967948

Suppliers and Price of Indol-1-yl-acetic acid ethyl ester

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

Total 2 raw suppliers

Chemical Property of Indol-1-yl-acetic acid ethyl ester

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:203.094628657
Heavy Atom Count:15
Complexity:230

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)CN1C=CC2=CC=CC=C21

Technology Process of Indol-1-yl-acetic acid ethyl ester

There total 1 articles about Indol-1-yl-acetic acid 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: 73.0%

: 623-73-4
diazoacetic acid ethyl ester

: 120-72-9
indole

: 778-82-5
ethyl 3-indoleacetate

: 1646144-91-3
diethyl 2,2'-(1H-indole-1,3-diyl)diacetate

: 61155-69-9
ethyl 2-(1H-indol-1-yl)acetate

Guidance literature:: With hydrotris(3,4,5-tribromo)pyrazolylborate Cu(NCMe); silica gel; In dichloromethane; at 30 ℃; for 3h; Schlenk technique; Inert atmosphere;
DOI:10.1002/cctc.201400097