phenyl 1H-indole-1-carboxylate

Base Information

Chemical Name:phenyl 1H-indole-1-carboxylate
CAS No.:74117-31-0
Molecular Formula:C15H11NO2
Molecular Weight:237.258
Hs Code.:
DSSTox Substance ID:DTXSID50446893
Nikkaji Number:J463.385G
Wikidata:Q82265639

Synonyms:phenyl 1H-indole-1-carboxylate;74117-31-0;1H-Indole-1-carboxylic acid, phenyl ester;1-Phenoxycarbonyl-1H-indole;DTXSID50446893;1H-indole-1-carboxylic acid phenyl ester

Suppliers and Price of phenyl 1H-indole-1-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of phenyl 1H-indole-1-carboxylate

Chemical Property:

PSA：31.23000
LogP:3.68840
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:237.078978594
Heavy Atom Count:18
Complexity:299

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OC(=O)N2C=CC3=CC=CC=C32

Technology Process of phenyl 1H-indole-1-carboxylate

There total 7 articles about phenyl 1H-indole-1-carboxylate 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: 100.0%

: 120-72-9
indole

: 1885-14-9
phenyl chloroformate

: 74117-31-0
phenyl 1H-indole-1-carboxylate

Guidance literature:: With sodium hydroxide; tetrabutylammomium bromide; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1016/j.tet.2004.07.071

Reference yield: 99.0%

: 102-09-0
bis(phenyl) carbonate

: 120-72-9
indole

: 74117-31-0
phenyl 1H-indole-1-carboxylate

Guidance literature:: With sodium carbonate; In acetonitrile; at 20 - 120 ℃; for 24h; Reagent/catalyst; Solvent; Temperature; regioselective reaction; Schlenk technique;
DOI:10.1080/00397911.2020.1758143