Benzyl 3-acetyl-1H-indole-1-carboxylate

Base Information

Chemical Name:Benzyl 3-acetyl-1H-indole-1-carboxylate
CAS No.:103871-32-5
Molecular Formula:C18H15NO3
Molecular Weight:293.322
Hs Code.:
DSSTox Substance ID:DTXSID70547396
Wikidata:Q82425589

Synonyms:N-Carbobenzoxy-3-acetyl indole;103871-32-5;Benzyl 3-acetyl-1H-indole-1-carboxylate;SCHEMBL9572545;DTXSID70547396;YMLWRJSPWWJKJE-UHFFFAOYSA-N

Suppliers and Price of Benzyl 3-acetyl-1H-indole-1-carboxylate

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Benzyl 3-acetyl-1H-indole-1-carboxylate

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:293.10519334
Heavy Atom Count:22
Complexity:417

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=CN(C2=CC=CC=C21)C(=O)OCC3=CC=CC=C3

Technology Process of Benzyl 3-acetyl-1H-indole-1-carboxylate

There total 1 articles about Benzyl 3-acetyl-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:

: 703-80-0
3-acetylindole

: 501-53-1,94274-21-2
benzyl chloroformate

: 103871-32-5
benzyl 3-acetyl-1H-indole-1-carboxylate

Guidance literature:: With sodium hydride; Yield given. Multistep reaction; 1.) THF, RT, 1 h, 2.) RT, overnight;
DOI:10.1021/jo00375a030

Reference yield: 89.0%

: 103871-32-5
benzyl 3-acetyl-1H-indole-1-carboxylate

: 103871-31-4,105311-49-7,105517-85-9
(+)-1-(N-carbobenzoxyindol-3-yl)ethanol

Guidance literature:: With lithium aluminium tetrahydride; (2R,3R)-4-dimethylamino-3-methyl-1,2-diphenyl-butan-2-ol; In diethyl ether; at -78 ℃; for 2h;
DOI:10.1021/jo00375a030